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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923483Generated: October 27, 2026

Water → tert-butyl {2-[(1S,2R)-1,2-dihydroxypropyl]benzyl}carbamate

https://huagongshe.com/reaction/923483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ThiosulfateHCID 24477—
ReactantMethanesulfonamideHCID 72879—
Reactanttert-butyl {2-[(1Z)-prop-1-en-1-yl]benzyl}carbamateHCID 118318066—
Solventtert-ButanolHCID 6386—
Producttert-butyl {2-[(1S,2R)-1,2-dihydroxypropyl]benzyl}carbamateHCID 118318079—

Reaction Steps

To a mixture of 3.30 g of AD mix-α, 200 mg of methanesulfonamide, 12.5 ml of tert-butyl alcohol, and 12.5 ml of water was added a solution of 500 mg of tert-butyl {2-[(1Z)-prop-1-en-1-yl]benzyl}carbamate in 5 ml of tert-butyl alcohol, followed by stirring at room temperature for 12 hours. To the reaction mixture was added sodium thiosulfate, followed by extraction with chloroform. The organic layer was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was then evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 449 mg of tert-butyl {2-[(1S,2R)-1,2-dihydroxypropyl]benzyl}carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278968B2
Source datasetuspto-grants-2016_03
ORD IDord-195099e262304b24bca2d9c68b8c5fec
Source noteuspto-grants-2016_03