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HRID 365271作成日:2026年10月26日

Benzyl Alcohol → Benzyl 6-bromohexanoate

https://huagongshe.com/reaction/365271

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物6-Bromohexanoyl chlorideHCID 89848—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物Benzyl 6-bromohexanoateHCID 562258—

反応手順

Benzyl 6-bromohexanoate was prepared by dropwise addition of a solution of 6-bromohexanoyl chloride (20.0 mL) in 100 mL of methylene chloride to a solution of 66.22 mL of benzyl alcohol in 60 mL of pyridine. The mixture was cooled using an ice-water bath for 90 min, then stirred at room temperature for 18 h. The solution was extracted with 200 mL of 1 N HCl followed by 2×150 mL of sat. NaHCO3. The extracts were discarded and the solution dried over Na2SO4. The solution was filtered and the solvent removed in vacuo to give an oil. This oil was purified on silica gel, eluting with a gradient of chloroform in hexanes. Fractions containing the product (TLC Rf 0.52, CHCl3 /hexanes 6:4) were combined and the solvent removed to give 24.4 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06127170
出典データセットuspto-grants-2000_10
ORD IDord-1568585a96fd44dd86799a68d94328fb
出典メモuspto-grants-2000_10