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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640005Generated: November 2, 2026

Ethanol → Ethyl 5-chloro-2-methylbenzoate

https://huagongshe.com/reaction/1640005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Chloro-2-methylbenzoic acidHCID 82009—
SolventDiethyl EtherHCID 3283—
ProductEthyl 5-chloro-2-methylbenzoateHCID 21269135—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 5-chloro-2-methylbenzoic acid (3.00 g, 17.5 mmol) in ethanol (30 mL) was cooled to 0° C. with an ice bath and thionyl chloride (12.5 mL, 105.5 mmol) was added dropwise, over 30 minutes. After this time, the mixture was warmed to room temperature for 1 h, then transferred to an oil bath, and heated to 70° C. overnight. The mixture was then cooled to room temperature and concentrated under reduced pressure. The solids obtained were then redissolved in diethyl ether (50 mL) and washed with 1 N sodium hydroxide (50 mL), brine (50 mL), dried over magnesium sulfate, and concentrated under reduced pressure to afford ethyl 5-chloro-2-methylbenzoate as a clear oil: 1H NMR (500 MHz, CDC13) δ 7.88 (d, J=2.5 Hz, 1H), 7.34 (dd, J=8.5, 2.5 Hz, 1H), 7.17 (d, J=8.5 Hz, 1H), 4.36 (q, J=7.5 Hz, 2H), 2.56 (s, 3H), 1.39 (t, J=7.5 Hz, 3H); ESI MS m/z 199 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110681B2
Source datasetuspto-grants-2012_02
ORD IDord-f3f4033727014c169a472b82ebe52a1c
Source noteuspto-grants-2012_02