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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714545Generated: October 30, 2026

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

https://huagongshe.com/reaction/1714545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
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-bromosuccinimide. The resulting solution was allowed to warn 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 numberUS07795448B2
Source datasetuspto-grants-2010_09
ORD IDord-d46f8ae9899f4d65b382f4f00936da42
Source noteuspto-grants-2010_09