反应 #4065669
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-cde5b1b4cc7c4e518ac20a23e34ef667暂无可渲染的结构数据
CC1CCC(CC1)CBr产品信息
1-(溴甲基)-4-甲基环己烷(CAS 78507-26-3)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 13460364
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
5 条反应 · 5 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-cde5b1b4cc7c4e518ac20a23e34ef667反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Methylcyclohexylmethyl bromide (3.1 g; 0.0164 M) was added dropwise to a refluxing solution of imidazole (1.12 g; 0.0165 M) in a solution of potassium tertiary butoxide (1.85 g; 0.0165 M) in n-butanol (50 cm3). The reaction mixture was kept under dry nitrogen. After addition the mixture was heated under reflux for a further 2 hours and stood overnight at room temperature. TLC showed reaction half complete. The mixture was refluxed for a further 8 hours and stood over weekend at room temperature. TLC showed no further reaction was occurring. Insoluble material was filtered off, and solvent removed under vacuum. Residue taken up in 2 N-HCl (100 cm3) and washed with ether (50 ml). Aqueous layer basified with excess 10 N NaOH and extracted with chloroform (3×50 cm3). Combined extracts were dried over anhydrous MgSO4 and solvent removed under vacuum. Oily residue was run on a silica gel column and eluted with EtOAc/MeOH 9:1. 0.8 g of column product obtained and was distilled to give 0.28 g of pure product having b.p. 80° C. at 0.125 mmHg. After addition the mixture was heated under reflux for a further 2 hours reaction half complete The mixture was refluxed for a further 8 hours stood over weekend at room temperature no further reaction Insoluble material was filtered off solvent removed under vacuum washed with ether (50 ml) extracted with chloroform (3×50 cm3) Combined extracts were dried over anhydrous MgSO4 and solvent removed under vacuum eluted with EtOAc/MeOH 9:1 0.8 g of column product obtained was distilled
来源 ID: ord-75fc7754ae994b6cb654d37b80d37d42反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-cde5b1b4cc7c4e518ac20a23e34ef667反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 1-Bromomethyl-4-methylcyclohexane (3.1 g, 0.0162 mol) was added dropwise to a stirred, boiling solution of imidazole (1.12 g, 0.0165 mol) and potassium t-butoxide (1.85 g, 0.0165 mol) in dry n-butanol, under dry nitrogen. After the addition, the reaction mixture was stirred and heated under reflux for 10 h. After the addition heated under reflux for 10 h.
来源 ID: ord-bfaef8f7ff4b434dbd9c733d1c1916f0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Methylcyclohexylmethyl bromide (3.1 g; 0.0164 M) was added dropwise to a refluxing solution of imidazole (1.12 g; 0.0165 M) in a solution of potassium tertiary butoxide (1.85 g; 0.0165 M) in n-butanol (50 cm3). The reaction mixture was kept under dry nitrogen. After addition the mixture was heated under reflux for a further 2 hours and stood overnight at room temperature. TLC showed reaction half complete. The mixture was refluxed for a further 8 hours and stood over weekend at room temperature. TLC showed no further reaction was occurring. Insoluble material was filtered off, and solvent removed under vacuum. Residue taken up in 2 N-HCl (100 cm3) and washed with ether (50 ml). Aqueous layer basified with excess 10 N NaOH and extracted with chloroform (3×50 cm3). Combined extracts were dried over anhydrous MgSO4 and solvent removed under vacuum. Oily residue was run on a silica gel column and eluted with EtOAc/MeOH 9:1. 0.8 g of column product obtained and was distilled to give 0.28 g of pure product having b.p. 80° C. at 0.125 mmHg. After addition the mixture was heated under reflux for a further 2 hours reaction half complete The mixture was refluxed for a further 8 hours stood over weekend at room temperature no further reaction Insoluble material was filtered off solvent removed under vacuum washed with ether (50 ml) extracted with chloroform (3×50 cm3) Combined extracts were dried over anhydrous MgSO4 and solvent removed under vacuum eluted with EtOAc/MeOH 9:1 0.8 g of column product obtained was distilled
来源 ID: ord-75fc7754ae994b6cb654d37b80d37d42PubChem References
以下资料来自该化合物的公开数据库参考记录。
相关产品
12 related records
CAS 1647-23-0
CAS 1647-26-3
CAS 30310-22-6
CAS 18908-66-2
CAS 31950-58-0
CAS 100516-81-2
CAS 3814-30-0
CAS 36982-56-6
CAS 10364-04-2
CAS 3814-34-4
CAS 2550-36-9
CAS 4549-33-1
