Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191607Generated: November 1, 2026

Water → 2-(2-Benzyloxy-6-methoxy-phenyl)-5,5-dimethyl-3-(4-phenoxy-benzyl)-oxazolidin-4-one

https://huagongshe.com/reaction/2191607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-(Bromomethyl)-4-phenoxybenzeneHCID 1514251—
Reactant2-(2-Benzyloxy-6-methoxy-phenyl)-5,5-dimethyl-oxazolidin-4-oneHCID 66789321—
SolventDimethylformamideHCID 6228—
SolventHeptaneHCID 8900—
Product2-(2-Benzyloxy-6-methoxy-phenyl)-5,5-dimethyl-3-(4-phenoxy-benzyl)-oxazolidin-4-oneHCID 6678896877.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) solution of 2-(2-benzyloxy-6-methoxy-phenyl)-5,5-dimethyl-oxazolidin-4-one (410 mg) in dry DMF (5 mL) is added portionwise NaH 90% (45 mg, 1.5 eq). The reaction mixture is stirred for 15 min at 0° C. and then commercially available 1-(bromomethyl)-4-phenoxybenzene (395 mg, 1.2 eq) is added and the reaction mixture is stirred at RT for 1 h. The reaction mixture is poured into water, extracted with DCM. The combined organic extracts are dried (MgSO4), filtered and concentrated to yield a crude oil. FC (EN n-heptane: 0/1 to 4/6) gives 2-(2-benzyloxy-6-methoxy-phenyl)-5,5-dimethyl-3-(4-phenoxy-benzyl)-oxazolidin-4-one as a colorless oil (0.495 g, 77%); LC-MS: tR=0.88 min; [M+H]+=510.33.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329706B2
Source datasetuspto-grants-2012_12
ORD IDord-a904b9763e72401fb5a3f4e9b459e6e9
Source noteuspto-grants-2012_12