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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844399Generated: November 2, 2026

Water → (R)-tert-butyl 1-bromopropan-2-ylcarbamate

https://huagongshe.com/reaction/1844399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-butyl N-((2R)-1-hydroxypropan-2-yl)carbamateHCID 13200309—
SolventDichloromethaneHCID 6344—
Product(R)-tert-butyl 1-bromopropan-2-ylcarbamateHCID 5708179250.1%

Reaction Steps

(R)-tert-Butyl 1-hydroxypropan-2-ylcarbamate (1 g, 5.71 mmol) and carbon tetrabromide (2.84 g, 8.56 mmol) were stirred in CH2Cl2 (20 mL) at −20° C. under argon. A solution of triphenylphosphine (2.40 g, 9.13 mmol) in CH2Cl2 (5 mL) was added dropwise. The reaction was allowed to reach rt and stirred for 14 h. H2O (50 mL) was added to the reaction mixture and the aqueous layer was removed and the CH2Cl2 layer was dried over Na2SO4, filtered, and evaporated. The residue was applied to a silica ISCO column and eluted with 5:1 hexanes/EtOAc. Intermediate 5A (0.68 g, 2.86 mmol, 50.0% yield) was isolated as a white solid. LC-MS (ESI) 183.9 (M−tBu+H), RT=1.76 min (Method B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946430B2
Source datasetuspto-grants-2015_02
ORD IDord-f5cce0b148ec4b1f8187b3a969ec9ea9
Source noteuspto-grants-2015_02