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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037433Generated: October 31, 2026

Oxolane--water (1/1) → HCID 66856356, compound

https://huagongshe.com/reaction/2037433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxolane--water (1/1)HCID 21881883—
ReactantHCID 66856823HCID 66856823—
CatalystOsmium TetroxideHCID 30318—
SolventEthyl AcetateHCID 8857—
ProductHCID 66856356HCID 66856356—

Reaction Steps

To a solution of 6-allyl-3-((S)-1-(2′,4′-difluorobiphenyl-4-yl)ethyl)-6-(4-fluorophenyl)-1,3-oxazinan-2-one (obtained as described in Example 111) in THF-H2O (1:1, 20 mL) were added NaIO4 (1.0148 g, 4.74 mmol, 5 equiv) and OsO4 (2.5 wt. % solution in t-BuOH, 0.1708 g, 0.0167 mmol, 0.018 equiv), and the mixture was stirred at rt for 2 h. The mixture was diluted with EtOAc, dried over Na2SO4, and concentrated under reduced pressure. The residue was dissolved in MeOH (10 mL) and NaBH4 (0.200 g) was added. After the mixture was stirred for 1 h at rt, acetone was added. The solvents were removed in vacuo, the residue was treated with saturated brine, extracted with CH2Cl2, and dried over Na2SO4. After the solvents were evaporated, the residue was purified by chromatography on silica gel eluted with hexanes/EtOAc to afford the two diastereomers of 3-((S)-1-(2′,4′-difluorobiphenyl-4-yl)ethyl)-6-(4-fluorophenyl)-6-(2-hydroxyethyl)-1,3-oxazinan-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575156B2
Source datasetuspto-grants-2013_11
ORD IDord-4c1d66a3054146fb9988259532b0a741
Source noteuspto-grants-2013_11