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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809142Generated: October 25, 2026

Ammonium Chloride → 2-(2-Bromopyridin-3-yl)-1-(3-chlorophenyl)ethanol

https://huagongshe.com/reaction/1809142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(2-Bromopyridin-3-yl)acetaldehydeHCID 58138967—
ReactantHCID 178478982HCID 178478982—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Bromopyridin-3-yl)-1-(3-chlorophenyl)ethanolHCID 5813893735%

Reaction Steps

To 2-(2-bromopyridin-3-yl)acetaldehyde (864 mg, 4.7 mmol) in THF (10 mL) at 0° C. was added (3-chlorophenyl)magnesium chloride (0.5M in THF, 14 mL, 7.04 mmol). The mixture was stirred at room temperature for 4 hours then treated with ammonium chloride (sat) at 0° C., extracted with ethyl acetate. The combined ethyl acetate layer was washed with brine, dried over magnesium sulfate and concentrated. Purification by chromatography on silica gel gave 2-(2-bromopyridin-3-yl)-1-(3-chlorophenyl)ethanol (490 mg, 35% yield) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362022B2
Source datasetuspto-grants-2013_01
ORD IDord-16f667542fb04a8cbfbd9c1e8bc7321c
Source noteuspto-grants-2013_01