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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38717Generated: October 26, 2026

Acetone → 4-(2,3-Dihydroxypropoxy)benzaldehyde

https://huagongshe.com/reaction/38717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethyl morpholine oxideHCID 82029—
Reactant4-(Allyloxy)benzaldehydeHCID 95942—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
Product4-(2,3-Dihydroxypropoxy)benzaldehydeHCID 16655848—

Reaction Steps

To a solution of 4-allyloxybenzaldehyde (1.0 g, 6.17 mmol) in acetone (40 mL) and water (5 mL) is added a 2.5% solution of OsO4 in tert. butanol (1.25 mL) followed by N-methyl morpholine-N-oxide (867 mg, 7.4 mmol). The pale yellow solution is stirred at rt for 6 h, diluted with EA (250 mL) and washed with 10% aq. citric acid solution (100 mL) and water (2×100 mL). The washings are extracted with EA (150 mL). The combined organic extracts are concentrated and purified by column chromatography on silica gel to give the title compound (731 mg) as a turbid oil. The title compound reversibly polymerizes upon standing. LC-MS: tR=0.58 min, [M+1+CH3CN]+=238.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524752B2
Source datasetuspto-grants-2013_09
ORD IDord-0e52fbecea614b5dbc1e4621228d68ef
Source noteuspto-grants-2013_09