Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705760Generated: October 31, 2026

Water → benzyl N-(4-bromo-2-ethylphenyl)carbamate

https://huagongshe.com/reaction/705760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
Reactant4-Bromo-2-ethylanilineHCID 2801283—
SolventTolueneHCID 1140—
Productbenzyl N-(4-bromo-2-ethylphenyl)carbamateHCID 71232504—

Reaction Steps

4-Bromo-2-ethylaniline (500 mg, 2.50 mmol) was dissolved in toluene (25 mL), sodium carbonate (397 mg, 3.75 mmol) and benzyl chloroformate (0.428 mL, 3.00 mmol) were added and the mixture stirred under nitrogen at room temperature. After 20 hours water (25 mL) was added, the aqueous phase separated and washed with ethyl acetate (2×25 mL). The combined organic extracts were washed with brine, dried over sodium sulfate and evaporated. Chromatography (40 g silica cartridge, 0-100% ethyl acetate/petroleum benzine 40-60° C.) gave the title compound (I38) (708 mg, 85%) as a pink solid; 1H NMR (400 MHz, CDCl3) δ 7.72 (s, 1H), 7.44-7.28 (m, 7H), 6.43 (s, 1H), 5.20 (s, 2H), 2.54 (q, J=7.6 Hz, 2H), 1.21 (t, J=7.6 Hz, 3H). LCMS Method C: rt 6.46 min; 258.0 [M-PhCH2O+CH3OH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174946B2
Source datasetuspto-grants-2015_11
ORD IDord-0c9c60f44436475aae1c25f7a8d8975c
Source noteuspto-grants-2015_11