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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365271Generated: October 25, 2026

Benzyl Alcohol → Benzyl 6-bromohexanoate

https://huagongshe.com/reaction/365271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant6-Bromohexanoyl chlorideHCID 89848—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductBenzyl 6-bromohexanoateHCID 562258—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127170
Source datasetuspto-grants-2000_10
ORD IDord-1568585a96fd44dd86799a68d94328fb
Source noteuspto-grants-2000_10