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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694903Generated: November 1, 2026

Ethyl Acetate → {2-[(2-Benzyloxyphenyl)-(2-bromoacetyl)amino]-1,1-dimethylethyl}carbamic acid t-butyl ester

https://huagongshe.com/reaction/1694903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBromoacetyl bromideHCID 61147—
ReactantSodium BicarbonateHCID 516892—
Reactant[2-(2-Benzyloxyphenylamino)-1,1-dimethylethyl]carbamic acid t-butyl esterHCID 66645956—
SolventWaterHCID 962—
Product{2-[(2-Benzyloxyphenyl)-(2-bromoacetyl)amino]-1,1-dimethylethyl}carbamic acid t-butyl esterHCID 6664539492.4%

Reaction Steps

1.08 g of sodium bicarbonate (12.9 mmol) and 1.0 ml of bromoacetyl bromide (11.3 mmol) were added to a solution of 4.00 g of [2-(2-benzyloxyphenylamino)-1,1-dimethylethyl]carbamic acid t-butyl ester obtained in Example (10a) (10.7 mmol) in a mixed solvent of ethyl acetate (50 ml) and water (50 ml) under ice-cooling, and the mixture was stirred at the same temperature for 10 minutes. After extraction with ethyl acetate, the organic layer was dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent:hexane/ethyl acetate=2/1) to obtain 4.86 g of the title compound (yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158790B2
Source datasetuspto-grants-2012_04
ORD IDord-3784cb5f8db34e28acbebc160b2b5f36
Source noteuspto-grants-2012_04