Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218228Generated: October 30, 2026

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

https://huagongshe.com/reaction/218228

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 numberUS08198331B2
Source datasetuspto-grants-2012_06
ORD IDord-8b58122e3aa142f682c9f941729e1a92
Source noteuspto-grants-2012_06