HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777373Generated: November 3, 2026
Sodium borohydride → HCID 118020562, compound
https://huagongshe.com/reaction/1777373
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 118201022 | HCID 118201022 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 118020562 | HCID 118020562 | — |
Reaction Steps
To a solution of (±)-ethyl 3-[5-methyl-2-(2H-1,2,3-triazol-2-yl)benzoyl]-1,3-oxazolidine-2-carboxylate obtained in Reference Example 1 (4.0 g, 12.1 mmol) in MeOH (60 mL), NaBH4 (4.6 g, 121 mmol) was added gradually under cooling with ice water and stirred for 1 hour. The resulting mixture was heated to room temperature and stirred for 1 hour. The solvent was distilled off under reduced pressure, a saturated aqueous solution of ammonium chloride was added to the reaction mixture, which was extracted with CHCl3. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over Na2SO4, then the drying agent was filtered off, and then the solvent was distilled off under reduced pressure. The obtained residue was purified by column chromatography (HP-Sil 100 g, hexane/EtOAc=88/12 to 0/100) to obtain the title compound (3.6 g) (colorless oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266870B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-b77589bcec714ef18f426eda7551c245 |
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| Source note | uspto-grants-2016_02 |
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