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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532789Generated: October 30, 2026

Methanol → Methyl 4-chlorophenylacetate

https://huagongshe.com/reaction/532789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant(4-Chlorophenyl)acetic acidHCID 15880—
CatalystSulfuric AcidHCID 1118—
ProductMethyl 4-chlorophenylacetateHCID 10419692%

Reaction Steps

A solution of 2-(4-chlorophenyl)acetic acid (20.0 g, 117 mmol) in dry methanol (235 mL) was treated with 5 drops of concentrated H2SO4 (cat.) at room temperature. The mixture was stirred overnight to completion, and then concentrated in vacuo to about 40 milliliters. The concentrate was partitioned between ether and half saturated NaHCO3 solution. The aqueous portion was back-extracted once with ether, and the organics were combined. The organic portion was washed with water, then brine, dried over MgSO4, and concentrated in vacuo. The material was placed under high vacuum for one hour to afford the pure methyl 2-(4-chlorophenyl)acetate as a pale yellow oil (19.8 g, 92%). 1H NMR (CDCl3, 400 MHz) δ 7.30 (d, J=8.4 Hz, 2H), 7.21 (d, J=8.4 Hz, 2H), 3.70 (s, 3H), 3.60 (2, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853199B2
Source datasetuspto-grants-2014_10
ORD IDord-823a0a98d783488bbe774516d2bb5dde
Source noteuspto-grants-2014_10