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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037427Generated: November 1, 2026

HCID 58109235, compound → HCID 58109535, compound

https://huagongshe.com/reaction/2037427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58109235HCID 58109235—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58109535HCID 58109535150.6%

Reaction Steps

To a solution of ethyl 2-(3-((S)-1-((R/S)-6-methyl-2-oxo-6-phenyl-1,3-oxazinan-3-yl)ethyl)phenoxy)acetate (0.0369 g, 0.0928 mmol) in THF (5 mL) was added methylmagnesium bromide (1.4 M in toluene/THF, 1.0 mL, 1.4 mmol) at rt under nitrogen. After stirring for 1 h, the mixture was quenched with saturated NH4Cl (1 mL), diluted 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 0.0268 g (75%) of (R/S)-3-((S)-1-(3-(2-hydroxy-2-methylpropoxy)phenyl)ethyl)-6-methyl-6-phenyl-1,3-oxazinan-2-one. LC-MS Method 1, tR=1.64 min, m/z=384 (M+1). 1H NMR (CDCl3) 7.41-7.23 (m, 6H), 6.92-6.88 (m, 2H), 6.84-6.81 (m, 1H), 5.77 (q, J=7.0 Hz, 1H), 3.78 (s, 2H), 2.70-2.67 (m, 2H), 2.29-2.24 (m, 1H), 2.23 (s, 1H), 2.06-1.98 (m, 1H), 1.64 (s, 3H), 1.35 (s, 6H), 1.27 (d, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575156B2
Source datasetuspto-grants-2013_11
ORD IDord-fe38c63138f243ae81e7b66b07ad2349
Source noteuspto-grants-2013_11