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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640790Generated: October 31, 2026

(S)-3-((S)-1-(4-bromophenyl)ethyl)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-1,3-oxazinan-2-one → 6-Phenyl-1,3-oxazinan-2-one

https://huagongshe.com/reaction/1640790

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-3-((S)-1-(4-bromophenyl)ethyl)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-1,3-oxazinan-2-oneHCID 44599033—
Reactant2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 44754862—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Product6-Phenyl-1,3-oxazinan-2-oneHCID 241005274.8%

Reaction Steps

A mixture of (S)-3-((S)-1-(4-bromophenyl)ethyl)-6-(2-hydroxy-2-methylpropyl) -6-phenyl-1,3-oxazinan-2-one (100 mg, 0.23 mmol), 2-methoxy-4-(4,4,5,5-tetramethyl -1,3,2-dioxaborolan-2-yl)pyridine (68 mg, 1.25 equiv), Pd(dppf)Cl2.CH2Cl2 (19 mg, 10% mol), 2M aq Na2CO3 (1 mL), 1,4-dioxane (3 mL) was degassed, refilled with N2 gas for 3 times before being put into microwave oven for 2 h at 130° C. LC-MS found the reaction was completed. The mixture was diluted with EtOAc (50 mL), washed with water (10 mL) and brine (8 mL), and dried over Na2SO4. After filtration and concentration, the residue was purified by chromatography on a 12-g silica gel column, eluted with a 0 to 10% MeOH in CH2Cl2 gradient to afford (S)-6-(2-hydroxy-2-methylpropyl)-3-(S)-1-(4-(2-methoxypyridin-4-yl)phenyl)ethyl)-6-phenyl-1,3-oxazinan-2-one (112 mg, quant yield). LC-MS Method 1 tR=1.66 min, m/z=461(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114868B2
Source datasetuspto-grants-2012_02
ORD IDord-a30b21255d9d45cfa3596bc54a8a4094
Source noteuspto-grants-2012_02