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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662942Generated: October 25, 2026

Water → 1-(5-Bromo-2-nitrophenyl)ethan-1-ol

https://huagongshe.com/reaction/1662942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant1-(5-Bromo-2-nitrophenyl)ethanoneHCID 12224157—
SolventDiethyl EtherHCID 3283—
Product1-(5-Bromo-2-nitrophenyl)ethan-1-olHCID 45073390—

Reaction Steps

In an ice bath, about 10 mmols of 3-acetyl-4-nitro-bromobenzene was put into a 100 mL two-neck round flask, dissolved in about 30 mL solvent ether, and sodium borohydride was gradually added. The solution was stirred at room temperature for about 2 hours. After confirming reaction completion using TLC, reaction was completed by using about 5 mL water. The precipitate was filtered, and the filtered solution was washed twice with sodium chloride solution (about 30 mL). Then the washed solution was dried with sodium sulfate anhydride, and distilled under reduced pressure. Then, 1-(5-bromo-2-nitrophenyl)ethanol was obtained in a form of about 71% yellow oil using silica gel column chromatography (Hexane/EtOAc=2/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034747B2
Source datasetuspto-grants-2011_10
ORD IDord-fe835b0527aa42208492638f15e4e440
Source noteuspto-grants-2011_10