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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502397Generated: October 25, 2026

5-Chloro-2-fluorobenzaldehyde → 1-(5-Chloro-2-fluorophenyl)propan-1-ol

https://huagongshe.com/reaction/1502397

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-fluorobenzaldehydeHCID 2773586—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
Product1-(5-Chloro-2-fluorophenyl)propan-1-olHCID 8398832171%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-chloro-2-fluorobenzaldehyde (1 g, 6.3 mmol) in diethyl ether (20 mL) cooled at −78° C. was added a solution of 3.0M ethylmagnesium bromide in ether (4.2 mL, 13 mmol) dropwise over 5 minutes. The reaction mixture was warmed to 0° C. and after 30 minutes was quenched with a few drops of saturated aqueous ammonium chloride solution. The reaction mixture was diluted with ethyl acetate (50 mL) and washed with water (50 mL). The organic layer was separated, dried over sodium sulfate, filtered, and evaporated in vacuo to afford a residue that was purified by flash chromatography (silica, 4 g, ISCO, 0-30% ethyl acetate in heptane) to afford the title compound as a pale yellow oil (850 mg, 71%), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206175B2
Source datasetuspto-grants-2015_12
ORD IDord-82ed36c19e184ef5b4953eb98e9ce4b2
Source noteuspto-grants-2015_12