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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910034Generated: October 27, 2026

Bromine → [4-Bromo-2-(2-bromoacetyl)phenoxy]acetic acid ethyl ester

https://huagongshe.com/reaction/910034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantEthyl 2-(2-acetyl-4-bromophenoxy)acetateHCID 19261366—
SolventChloroformHCID 6212—
Product[4-Bromo-2-(2-bromoacetyl)phenoxy]acetic acid ethyl esterHCID 5765880194%

Reaction Steps

To a cooled (0° C.) solution of (2-acetyl-4-bromophenoxy)acetic acid ethyl ester (2.5 g, 8.3 mmol) in CHCl3 (25 mL) was slowly added bromine (425 uL, 8.3 mmol). After completion the reaction mixture was allowed to stir at room temperature for 1 hour. The mixture was partitioned between CH2Cl2 and brine. The organic phase was washed with brine, dried (MgSO4) and concentrated in vacuo to give the title compound as a white solid (2.97 g, 7.8 mmol, 94%): 1H NMR (CDCl3): δ 1.35 (t, 3H), 4.32 (q, 2H), 4.75 (s, 2H), 4.76 (s, 2H), 6.77 (d, 1H), 7.60 (dd, 1H), 7.97 (s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022063B2
Source datasetuspto-grants-2011_09
ORD IDord-362a6e885afd4e0ab0c31f51c8644df9
Source noteuspto-grants-2011_09