反应 #4136174
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-23a04c29288740ca9e134c48c99ecf53暂无可渲染的结构数据
COC(=O)CCCCCCCBr产品信息
8-溴辛酸甲酯(CAS 26825-92-3)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。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-23a04c29288740ca9e134c48c99ecf53反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b29babbed6424607a076f33edff3588b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9e572b3acde1482cb8b61730f75edb4d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6b3c481f8bbf482ab746ed342fe16402反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6b353c95bfe8400c9bc8da5e31e59aab反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e67b8344a20349fd816e1fac34519307反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The product is produced as described in example 1 from 0.75 g. of NaH (80% suspension in mineral oil), 5.6 g. of 1-benzylbenzimidazolin-2-one (produced in usual manners by alkylation of benzimidazolin-2-one with benzylchloride according to example 8), 50 cc. of DMF, 5.9 g. of 8-bromocaprylic acid methyl ester and 0.75 g. of NaJ. The product is produced
来源 ID: ord-fdb769078caf46fbb94c01b9cc831d09反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The product is produces as described in example 1 from 1.2 g. of NaH (80% suspension in mineral oil), 9.8 g. of 1-(3-chlorophenyl)-benzimidazolin-2-one, 80 cc. of DMF, 9.5 g. of 8-bromocaprylic acid methyl ester and 1.2 g. of NaJ. The product is produces
来源 ID: ord-7468b507969d40f5a1f52fd93840d01c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The product is produced as described in example 1 from 0.9 g. of NaH (80% suspension in mineral oil), 7.5 g. of 1-octylbenzimidazolin-2-one (produced) by alkylation from benzimidazolin-2-one with bromooctane according to example 8), 100 cc. of DMF, 7.1 g. of 8-bromocaprylic acid methyl ester and 0.9 g. of NaJ. Eluant in chromatographic purification: hexane/ethylacetate. The product is produced Eluant in chromatographic purification
来源 ID: ord-cb6ba25dbe284f008800d616d4b95ef7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The product is produced as described in example 1 from 2.8 g. of NaH (80% suspension in mineral oil), 25 g. of benzimidazolin-2-one, 180 cc. of DMF, 22.1 g. of 8-bromocaprylic acid methyl ester and 2.8 g. of NaJ. Eluant in chromatographic purification: chloroform/methanol. The product is produced Eluant in chromatographic purification
来源 ID: ord-fefd9dabde024563a0c8f52b4a7146f2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The product is produced as described in example 1 from 3 g. of NaH (80% suspension in mineral oil), 15.1 g. of benzthiazolin-2-one, 200 cc. of DMF, 23.7 g. of 8-bromo-caprylic acid methyl ester and 3 g. NaJ. The product is produced
来源 ID: ord-addf4e48275b4874a28b8f3d64b11e27反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The product is produced as described in example 1 from 3 g. of NaH (80% suspension in mineral oil), 17 g. of 5-chloro-benzoxazolin-2-one (produced in usual manners by subjecting 2-amino-4-chloro-phenol-hydrochloride to reaction with phosgene), 200 cc. of DMF, 23.7 g. of 8-bromo-caprylic acid methyl ester and 3 g. of NaJ. The product is produced
来源 ID: ord-1276cb9699e947f78b4dcbe8f2f4cf38PubChem References
以下资料来自该化合物的公开数据库参考记录。
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