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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261432Generated: November 3, 2026

Water → 3-(4-Bromophenyl)propane-1,2-diol

https://huagongshe.com/reaction/2261432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl morpholine oxideHCID 82029—
ReactantBenzene, 1-bromo-4-(2-propenyl)-HCID 137529—
CatalystOsmium TetroxideHCID 30318—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
Product3-(4-Bromophenyl)propane-1,2-diolHCID 20332740—

Reaction Steps

A solution of 1-allyl-4-bromo-benzene (2.0 g, 10.2 mmol) in acetone (60 mL) is treated with OsO4 (52 mg, 0.20 mmol), NMO (1.44 g, 12.2 mmol) and water (approx. 0.3 mL). The clear solution is stirred at rt for 2 h, diluted with DCM (150 mL) and washed twice with 10% aq. citric acid (2×75 mL). The aqueous phase is extracted twice with DCM. The organic extracts are combined, dried over MgSO4 and evaporated. The crude product is purified by CC on silica gel eluting with EA to give 3-(4-bromo-phenyl)-propane-1,2-diol (1.41 g) as an almost colourless oil; LC-MS: tR=0.72 min; 1H NMR (CDCl3): δ 7.46-7.40 (m, 2H), 7.14-7.08 (m, 2H), 3.96-3.87 (m, 1H), 3.73-3.67 (m, 1H), 3.55-3.47 (m, 1H), 2.81-2.67 (m, 2H), 1.90 (s br, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846964B2
Source datasetuspto-grants-2010_12
ORD IDord-c57af3846a0d42c986fffa12a24cd2ab
Source noteuspto-grants-2010_12