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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500150Generated: November 2, 2026

Triethylamine hydrochloride → P-Chloroacetophenone

https://huagongshe.com/reaction/1500150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantDimethylacetamideHCID 31374—
ReactantMethyl (4-chlorobenzoyl)acetateHCID 735885—
ReactantSodium bicarbonate waterHCID 86585896—
SolventEthyl AcetateHCID 8857—
ProductP-ChloroacetophenoneHCID 7467—

Reaction Conditions

Temperature140 °C

Reaction Steps

In 3-(4-chlorophenyl)-3-oxopropionic acid methyl ester (1.0 g, 0.0047 mol), N,N-dimethylacetamide (1 mL) and triethylamine hydrochloride (0.97 g, 0.0047×1.5 mol) were added and stirred at 140° C. for 3 hours under an argon atmosphere. In the reaction liquid, ethyl acetate and saturated sodium bicarbonate water were added, and the mixture was partitioned. After extracting the aqueous layer using ethyl acetate, the organic layer was dried using anhydrous sodium sulfate and concentrated. Thereafter, the dried and concentrated product was purified using a silica gel column, and a target product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206106B2
Source datasetuspto-grants-2015_12
ORD IDord-ea251da7148742fc8ace14f8bd71257d
Source noteuspto-grants-2015_12