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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545454Generated: October 29, 2026

Water → tert-butyl 2-(4-bromophenyl)acetate

https://huagongshe.com/reaction/545454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoron trifluoride etherateHCID 8000—
Reactanttert-Butyl acetateHCID 10908—
ReactantBenzeneacetic acid, 4-bromo-HCID 74654—
Producttert-butyl 2-(4-bromophenyl)acetateHCID 14775457—

Reaction Steps

To a solution of 4-bromophenylacetic acid (5.00 g, 23.2 mmol) in tBuOAc (75 mL) was added BF3.OEt2 (2.95 mL, 23.2 mmol). The mixture was allowed to stir overnight at room temperature and poured into H2O. The aqueous phase was extracted with EtOAc. The organic phase was washed with sat. aq NaHCO3, dried over anhydrous Na2SO4, and concentrated in vacuo. Purification by flash chromatography on silica gel (0% to 100% EtOAc in hexanes) provided the title compound. 1H NMR (500 MHz, CDCl3): δ 7.48 (d, J=8.0 Hz, 2 H), 7.19 (d, J=8.0 Hz, 2 H), 3.52 (s, 2 H), 1.48 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935713B2
Source datasetuspto-grants-2011_05
ORD IDord-33e8eddae4f44679b6271562d3073c7a
Source noteuspto-grants-2011_05