HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206190Generated: November 3, 2026
Hydrochloric Acid → HCID 131735840, compound
https://huagongshe.com/reaction/2206190
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Oxazolidinone | HCID 73949 | — |
| Reactant | 4-(Bromomethyl)phenylboronic acid | HCID 2735593 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131735840 | HCID 131735840 | 53.1% |
Reaction Steps
To a solution of oxazolidin-2-one (243 mg) in anhydrous DMF (10 mL) was added sodium hydride (60% dispersion in mineral oil, 140 mg) in small portions under ice-cooling. The reaction mixture was stirred at room temperature for 2 hr, to the reaction mixture was added (4-(bromomethyl)phenyl)boronic acid (500 mg), and the mixture was stirred for 60 hr. To the reaction mixture was added ice water, and the aqueous layer was neutralized with 1N hydrochloric acid under ice-cooling, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was washed with diisopropyl ether and ethyl acetate to give the title compound (273 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371320B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-e37e975252d2424ea7952aeb555efa3e |
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| Source note | uspto-grants-2016_06 |
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