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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222878Generated: October 30, 2026

N-Bromosuccinamide → 1,1-dimethylethyl ((1S)-1-{[4-(bromoacetyl)phenyl]methyl}-3-hydroxypropyl)carbamate

https://huagongshe.com/reaction/222878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BromosuccinamideHCID 9834204—
Reactant1,1-dimethylethyl [(1S)-1-({4-[1-(ethyloxy)ethenyl]phenyl}methyl)-3-hydroxypropyl]carbamateHCID 57594583—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1,1-dimethylethyl ((1S)-1-{[4-(bromoacetyl)phenyl]methyl}-3-hydroxypropyl)carbamateHCID 57594732100%

Reaction Steps

To a cooled (0° C.) solution of 1,1-dimethylethyl [(1S)-1-({4-[1-(ethyloxy)ethenyl]phenyl}methyl)-3-hydroxypropyl]carbamate (15 g, 44 mmol) in tetrahydrofuran (450 mL) and water (150 mL) was added N-bromosuccinamide. The resulting solution was allowed to warm to room temperature and maintained for 90 minutes. The reaction was then concentrated and diluted with ethyl acetate (1 L). The resulting solution was washed with water (1 L) and brine (500 mL), dried (MgSO4) and concentrated to give 19.5 g (˜100%) of 1,1-dimethylethyl ((1S)-1-{[4-(bromoacetyl)phenyl]methyl}-3-hydroxypropyl)carbamate as a slightly yellow solid. ESMS [M+H]+: 386.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207340B2
Source datasetuspto-grants-2012_06
ORD IDord-466e84f984074ffd9e9029721709f653
Source noteuspto-grants-2012_06