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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403599Generated: November 2, 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/403599

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 numberUS08748444B2
Source datasetuspto-grants-2014_06
ORD IDord-61b659c3b56e49f2b3b5cf67577ef631
Source noteuspto-grants-2014_06