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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675886Generated: November 2, 2026

Methanol → Methyl 4-chlorophenylacetate

https://huagongshe.com/reaction/1675886

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 was concentrated in vacuo to about 40 mL. The concentrate was partitioned between an 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 numberUS08003651B2
Source datasetuspto-grants-2011_08
ORD IDord-690d08bc950f43ab8ba11b2e34af8dfb
Source noteuspto-grants-2011_08