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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432169Generated: October 25, 2026

Benzyl chloroformate → benzyl N-(4-bromo-2-methoxyphenyl)carbamate

https://huagongshe.com/reaction/432169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactant4-Bromo-2-methoxyanilineHCID 459257—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Productbenzyl N-(4-bromo-2-methoxyphenyl)carbamateHCID 2234683774.3%

Reaction Steps

A solution of sodium bicarbonate (3.12 g, 0.0371 mol) in water (35 mL) was added to a solution of 4-bromo-2-methoxyaniline (3.00 g, 0.0148 mol) in dioxane (50 mL). The resulting mixture was stirred for 5 minutes and benzyl chloroformate (3.8 g, 0.022 mol) was added dropwise over 3 minutes. The reaction mixture was for two hours, then dioxane was removed under reduced pressure and the water phase was extracted twice with ethyl acetate (100 mL each). The combined organic extracts were dried over magnesium sulfate and after filtration concentrated under reduced pressure. The resulting residue was purified by flash chromatography on silica using ethyl acetate/n-heptane (5:95) as mobile phase to yield benzyl N-(4-bromo-2-methoxyphenyl)carbamate (3.75 g, 0.011 mol) as a white solid: 1H NMR (DMSO-d6, 400 MHz) 8.72 (s, 1H), 7.61 (d, 1H), 7.38 (m, 5H), 7.20 (s, 1H), 7.10 (d, 1H), 5.14 (s, 2H), 3.81 (s, 3H). TLC (ethyl acetate/heptane 1:9) Rf 0.21.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660744B1
Source datasetuspto-grants-2003_12
ORD IDord-711581551b3f4498b6a374c6f81df232
Source noteuspto-grants-2003_12