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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(Bromomethyl)-4-phenoxybenzene | HCID 1514251 | — |
| Reactant | 2-(2-Benzyloxy-6-methoxy-phenyl)-5,5-dimethyl-oxazolidin-4-one | HCID 66789321 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 2-(2-Benzyloxy-6-methoxy-phenyl)-5,5-dimethyl-3-(4-phenoxy-benzyl)-oxazolidin-4-one | HCID 66788968 | 77.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329706B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-a904b9763e72401fb5a3f4e9b459e6e9 |
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| Source note | uspto-grants-2012_12 |
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