反应 #4092978
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-af5370cdb6584606aac6649925b7d422暂无可渲染的结构数据
BrCCCCCCCCCO[Si](C)(C)C(C)(C)C产品信息
氟维司群杂质10(CAS 149051-24-1)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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合成路线数据
7 条反应 · 7 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-af5370cdb6584606aac6649925b7d422反应条件: temp:-30.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5.2 cm3 of a solution of magnesium compound (0.42 M/l) prepared from the product obtained in Stage A and 2.3 cm3 of tetrahydrofuran is cooled down to 0°/+2° C. 30 mg of copper chloride is added, agitation is carried out for 30 minutes, followed by cooling down to −30° C. and 330 mg of 3-ethylenedioxy 5 (10-epoxy estr-9(11)-ene-17-one dissolved in 2 cm3 of tetrahydrofuran is added and agitation is carried out for 45 minutes. 6 cm3 of 2M hydrochloric acid is added and agitation is carried out for 2 hours at ambient temperature. The reaction medium is poured into a saturated aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate, washing with salt water, drying and evaporating the solvent. After chromatographing the residue on silica (eluant: ethyl acetate-cyclohexane 6-4), 192 mg of expected product is obtained. is cooled down to 0°/+2° C is added agitation is carried out for 45 minutes agitation is carried out for 2 hours at ambient temperature followed by extraction with ethyl acetate washing with salt water drying evaporating the solvent
来源 ID: ord-0271b8ed75bd4fed965fc92500715696反应条件: temp:-30.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5.2 cm3 of a solution of magnesium compound (0.42 M/l) prepared from the product obtained in Stage A and 2.3 cm3 of tetrahydrofuran is cooled down to 0°/+2° C. 30 mg of copper chloride is added, agitation is carried out for 30 minutes, followed by cooling down to −30° C. and 330 mg of 3-ethylenedioxy 5 (10-epoxy estr-9(11)-ene-17-one dissolved in 2 cm3 of tetrahydrofuran is added and agitation is carried out for 45 minutes. 6 cm3 of 2M hydrochloric acid is added and agitation is carried out for 2 hours at ambient temperature. The reaction medium is poured into a saturated aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate, washing with salt water, drying and evaporating the solvent. After chromatographing the residue on silica (eluant: ethyl acetate-cyclohexane 6-4), 192 mg of expected product is obtained. is cooled down to 0°/+2° C is added agitation is carried out for 45 minutes agitation is carried out for 2 hours at ambient temperature followed by extraction with ethyl acetate washing with salt water drying evaporating the solvent
来源 ID: ord-0271b8ed75bd4fed965fc92500715696反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-af5370cdb6584606aac6649925b7d422反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Tert-butyl-dimethylsilyl chloride (28.16 g, 186.8 mmol) was added in portions to a solution of 9-bromo-nonan-1-ol (27.8 g, 124.6 mmol) and imidazole (25.4 g, 373 mmol) in dry DCM (400 mL) at −10° C. under a nitrogen atmosphere. The reaction mixture was allowed to warm to RT overnight. The solids were removed by filtration and the filtrate was washed with 10% citric acid (aq), then brine, dried (MgSO4), filtered, and concentrated to dryness to afford the title compound as a yellow oil. The solids were removed by filtration the filtrate was washed with 10% citric acid (aq) brine, dried (MgSO4) filtered concentrated to dryness
来源 ID: ord-3bdea13b4c9e4a13a3abe82fea508bcb反应条件: temp:-30.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5.2 cm3 of a solution of magnesium compound (0.42 M/l) prepared from the product obtained in Stage A and 2.3 cm3 of tetrahydrofuran is cooled down to 0°/+2° C. 30 mg of copper chloride is added, agitation is carried out for 30 minutes, followed by cooling down to −30° C. and 330 mg of 3-ethylenedioxy 5 (10-epoxy estr-9(11)-ene-17-one dissolved in 2 cm3 of tetrahydrofuran is added and agitation is carried out for 45 minutes. 6 cm3 of 2M hydrochloric acid is added and agitation is carried out for 2 hours at ambient temperature. The reaction medium is poured into a saturated aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate, washing with salt water, drying and evaporating the solvent. After chromatographing the residue on silica (eluant: ethyl acetate-cyclohexane 6-4), 192 mg of expected product is obtained. is cooled down to 0°/+2° C is added agitation is carried out for 45 minutes agitation is carried out for 2 hours at ambient temperature followed by extraction with ethyl acetate washing with salt water drying evaporating the solvent
来源 ID: ord-47d30ecd2fa447e8a13253c50217bc99反应条件: temp:-30.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5.2 cm3 of a solution of magnesium compound (0.42 M/l) prepared from the product obtained in Stage A and 2.3 cm3 of tetrahydrofuran is cooled down to 0°/+2° C. 30 mg of copper chloride is added, agitation is carried out for 30 minutes, followed by cooling down to −30° C. and 330 mg of 3-ethylenedioxy 5 (10-epoxy estr-9(11)-ene-17-one dissolved in 2 cm3 of tetrahydrofuran is added and agitation is carried out for 45 minutes. 6 cm3 of 2M hydrochloric acid is added and agitation is carried out for 2 hours at ambient temperature. The reaction medium is poured into a saturated aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate, washing with salt water, drying and evaporating the solvent. After chromatographing the residue on silica (eluant: ethyl acetate-cyclohexane 6-4), 192 mg of expected product is obtained. is cooled down to 0°/+2° C is added agitation is carried out for 45 minutes agitation is carried out for 2 hours at ambient temperature followed by extraction with ethyl acetate washing with salt water drying evaporating the solvent
来源 ID: ord-0271b8ed75bd4fed965fc92500715696PubChem References
以下资料来自该化合物的公开数据库参考记录。
