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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494114Generated: October 30, 2026

Bromoacetyl bromide → HCID 131727451, compound

https://huagongshe.com/reaction/494114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantSodium BicarbonateHCID 516892—
ReactantCarbamic acid, [(1S)-2-(ethylamino)-1-methylethyl]-, 1,1-dimethylethyl esterHCID 99965190—
SolventEthyl AcetateHCID 8857—
ProductHCID 131727451HCID 131727451—

Reaction Steps

To a cold (0° C.) stirred solution of tert-butyl[(1S)-2-(ethylamino)-1-methylethyl]carbamate (11.0 g, 54.6 mmol) in a mixture of ethyl acetate (107 mL) and saturated aqueous sodium bicarbonate (65 mL), bromoacetyl bromide (12.1 g, 60.0 mmol) was added portionwise under an atmosphere of nitrogen. The mixture was allowed to warm up to room temperature over a period of 3.5 hours. The organic phase was separated, washed successively with saturated aqueous sodium bicarbonate, and brine. The organic extract was dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was concentrated as a solution in toluene under vacuum to afford the title compound. ES MS M+1=323, 325.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538112B2
Source datasetuspto-grants-2009_05
ORD IDord-64dd112132bb4c36a34ed600cbca2250
Source noteuspto-grants-2009_05