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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037415Generated: November 1, 2026

Sodium hydride → 3-(3-Bromobenzyl)-6-methyl-6-phenyl-1,3-oxazinan-2-one

https://huagongshe.com/reaction/2037415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Bromobenzyl bromideHCID 69979—
Reactant6-Methyl-6-phenyl-1,3-oxazinan-2-oneHCID 53474282—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Bromobenzyl)-6-methyl-6-phenyl-1,3-oxazinan-2-oneHCID 2518241932%

Reaction Steps

A solution of 6-methyl-6-phenyl-1,3-oxazinan-2-one (500 mg, 2.62 mmol) and NaH (189 mg, 7.86 mmol) in dry THF (10 mL) was stirred for 1 h. A solution of m-bromobenzyl bromide (1.31 g, 5.24 mmol) in dry THF (3 mL) was added. The mixture was stirred overnight at rt. The reaction mixture was quenched water and extracted with EtOAc. The organic layer was washed with brine, dried over Na2SO4, concentrated and purified by preparative TLC to afford 3-(3-bromobenzyl)-6-methyl-6-phenyl-1,3-oxazinan-2-one (300 mg, 32%). 1H NMR (CDCl3): 1.60-1.70 (s, 3H), 2.15-2.30 (m, 1H), 2.35-2.48 (m, 1H), 2.79-2.90 (m, 1H), 3.00-3.10 (m, 1H), 4.30-4.40 (m, 1H), 4.50-4.60 (m, 1H), 6.90-7.00 (m, 1H), 7.00-7.10 (m, 1H), 7.20-7.45 (m, 7H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575156B2
Source datasetuspto-grants-2013_11
ORD IDord-c4c12095ae4d47a99d1836af690e964f
Source noteuspto-grants-2013_11