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HRID 347796生成日期:2026年10月23日

一甲胺 → N-(4-甲氧基苄基)-N-甲胺

https://huagongshe.com/zh-CN/reaction/347796

反应方程式

参与物

角色名称HCID投料
反应物一甲胺HCID 6329—
反应物大茴香醛HCID 31244—
反应物硼氢化钠HCID 4311764—
溶剂乙醇HCID 702—
产物N-(4-甲氧基苄基)-N-甲胺HCID 485407—

反应步骤

A mixture of p-methoxybenzaldehyde (25 ml; 200 mmol) and 8M methylamine in ethanol (100 ml; 800 mmol) in 100 ml of ethanol was stirred at rt for 18 hours. After removing the volatiles in vacuo, the residue was dissolved in 300 ml of fresh ethanol and sodium borohydride (8.5 g; 225 mmol) was added portionwise over 1.5 hr. Following the addition, the reaction mixture was concentrated to ˜⅓ volume and water (50 ml) was added. After cooling in an ice bath, the stirred mixture was carefully acidified to pH ˜2 with 5% aqueous H2SO4. After stirring 15 minutes, the mixture was basified to pH 14 with 6N NaOH and extracted with ethyl ether (400 ml). The ether layer was washed with water (200 ml), brine (100 ml) and dried over MgSO4. Concentration afforded 28.04 g (93%) of B51.1 as a colorless liquid. (M+H)+=152.13 (HPLC>94%).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US07176214B2
来源数据集uspto-grants-2007_02
ORD IDord-951d120e73cb4074bdc7c86d69986e09
来源说明uspto-grants-2007_02