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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443524Generated: October 30, 2026

(3-Bromophenyl)acetic acid → Methyl 2-(3-bromophenyl)acetate

https://huagongshe.com/reaction/1443524

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Bromophenyl)acetic acidHCID 74653—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventMethanolHCID 887—
ProductMethyl 2-(3-bromophenyl)acetateHCID 11746402—

Reaction Steps

A solution of 3-bromophenylacetic acid (2.0 g, 9.3 mmol) and 4-dimethylamino pyridine (1.1 g, 9.3 mmol) in methanol (20 mL) was treated with N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDAC) (2.1 g, 11 mmol). Reaction stirred for 16 hours at room temperature. The reaction mixture was concentrated under reduced pressure. The residue was taken up in ethyl acetate and washed with water, saturated sodium bicarbonate, 1N phosphoric acid, and brine before drying over Na2SO4, filtering, and concentrating under reduced pressure to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE041135E1
Source datasetuspto-grants-2010_02
ORD IDord-62191d12dd8c40868fab0a0506fa89c4
Source noteuspto-grants-2010_02