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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091536Generated: November 1, 2026

6-allyl-3-((S)-3-(tert-butyldimethylsilyloxy)-3-methylbutan-2-yl)-6-phenyl-1,3-oxazinan-2-one → 6-allyl-3-((S)-3-hydroxy-3-methylbutan-2-yl)-6-phenyl-1,3-oxazinan-2-one

https://huagongshe.com/reaction/2091536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-allyl-3-((S)-3-(tert-butyldimethylsilyloxy)-3-methylbutan-2-yl)-6-phenyl-1,3-oxazinan-2-oneHCID 58485264—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product6-allyl-3-((S)-3-hydroxy-3-methylbutan-2-yl)-6-phenyl-1,3-oxazinan-2-oneHCID 42642396—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 6-allyl-3-((S)-3-(tert-butyldimethylsilyloxy)-3-methylbutan-2-yl)-6-phenyl-1,3-oxazinan-2-one isomer 1 (80 mg, 0.19 mmol) in 20% TFA/DCM (2 mL) was stirred for 30 min at 0° C. The mixture was concentrated to give crude 6-allyl-3-((S)-3-hydroxy-3-methylbutan-2-yl)-6-phenyl-1,3-oxazinan-2-one isomer 1 (50 mg, 86%). LC-MS Method 2 tR=1.85 min, m/z=326, 304; 1H NMR (CDCl3) 1.07 (m, 6H), 1.18 (s, 3H), 2.15 (m, 1H), 2.25 (m, 1H), 2.58 (m, 2H), 2.90 (m, 1H), 3.08 (m, 1H), 3.20 (m, 1H), 5.02 (m, 2H), 5.68 (m, 1H), 7.22 (3H), 7.31 (2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440658B2
Source datasetuspto-grants-2013_05
ORD IDord-af0d3aaa9f4f4dc6bbb677631be96550
Source noteuspto-grants-2013_05