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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920811Generated: October 26, 2026

Diethyl Ether → 1-(2-Bromo-3-chloro phenyl)butan-1-ol

https://huagongshe.com/reaction/1920811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-3-chlorobenzaldehydeHCID 23463927—
ReactantHCID 178455855HCID 178455855—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Bromo-3-chloro phenyl)butan-1-olHCID 5857279262%

Reaction Steps

Under an argon atmosphere, zinc chloride (0.68 g, 4.97 mmol) was added to a 2.0 M solution of n-propyl magnesium chloride in diethyl ether (12.42 mL, 24.93 mmol), and the mixture was stirred at room temperature. After stirring for 0.5 hours, a solution of 2-bromo-3-chlorobenzaldehyde (4.36 g, 19.87 mmol), which had been obtained in Reference example 7 (7b), in tetrahydrofuran (10 mL) was added dropwise thereto. After stirring for 2 hours under ice cooling, a saturated aqueous ammonium chloride solution (20 mL) was added thereto. The mixture obtained was extracted with ethyl acetate (20 mL×2). After that, the organic layers were washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (n-hexane/ethyl acetate=5/1) to give the title compound as a white solid (3.23 g, yield 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173631B2
Source datasetuspto-grants-2012_05
ORD IDord-2ad3a5a76dfb4a1b81282cf71787cfd4
Source noteuspto-grants-2012_05