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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039702Generated: October 26, 2026

Water → HCID 67270991, compound

https://huagongshe.com/reaction/1039702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-ButanolHCID 6386—
ReactantSodium SulfiteHCID 24437—
ReactantMethyl morpholine oxideHCID 82029—
Reactanttert-butyl (1S,2R)-1-fluoro-1-phenylbut-3-en-2-ylcarbamateHCID 86635707—
CatalystOsmiumHCID 23937—
ProductHCID 67270991HCID 67270991—

Reaction Conditions

Temperature23 °C

Reaction Steps

To a 250 mL RBF containing tert-butyl (1S,2R)-1-fluoro-1-phenylbut-3-en-2-ylcarbamate (105.00 mg, 396 mmol)(mixture of diasteromers at benzylic fluoride stereocenter) was added tert-butanol (3 mL) and water (1 ml). The mixture was allowed to stir at 23° C. for 2 min, then NMO (139 mg, 1187 mmol) and osmium tetraxide (124 μA, 396 mmol) were added and the reaction was allowed to stir for another 48 h. before the reaction was quenched with water and sodium sulfite (1496 mg, 11872 mmol). The reaction was allowed to stir for 15 min and then extracted with EtOAc (3×). The combined organics were washed with HCl (1 N), sodium bicarbonate, brine and dried over sodium sulfate. The dried solution was passed through a plug of silica gel and concentrated to give 102 mg of a colorless oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552181B2
Source datasetuspto-grants-2013_10
ORD IDord-fc1aa90153f141789ea0a6c8dcf5e13c
Source noteuspto-grants-2013_10