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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506424Generated: October 31, 2026

Water → 7-(1,2-Dihydroxyethyl)chroman-4-one

https://huagongshe.com/reaction/1506424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl morpholine oxideHCID 82029—
ReactantHCID 22323781HCID 22323781—
CatalystWaterHCID 962—
CatalystOsmium TetroxideHCID 30318—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product7-(1,2-Dihydroxyethyl)chroman-4-oneHCID 6717112799%

Reaction Steps

To a mixture of 7-vinylchroman-4-one (Preparation 2D, 0.801 g, 4.60 mmol) and a 50% solution of NMO in water (0.953 mL, 4.60 mmol) in THF (11 mL) at room temperature was added a 4% aqueous solution of osmium tetroxide in water (1.44 mL, 0.184 mmol). The reaction mixture was stirred at room temperature overnight. The reaction mixture was diluted with dichloromethane (200 mL) and washed with water (40 mL). The organic layer was collected and was washed with brine (40 mL). The combined aqueous layers were extracted with dichloromethane (200 mL), and the combined organic layers were dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded 7-(1,2-dihydroxyethyl)chroman-4-one (0.950 g, 4.56 mmol, 99% yield) as a dark yellow oil. The product had an HPLC ret. time=0.587 min.−Column: Chromolith SpeedROD 4.6×50 mm (4 min.); Solvent A=10% MeOH, 90% H2O, 0.1% TFA; Solvent B=90% MeOH, 10% H2O, 0.1% TFA. LC/MS M+1=209.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216972B2
Source datasetuspto-grants-2015_12
ORD IDord-2a0bd4899ef741ae987f31703fc7c41c
Source noteuspto-grants-2015_12