HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280699Generated: October 27, 2026
Sodium borohydride → HCID 70981793, compound
https://huagongshe.com/reaction/2280699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Cerium trichloride heptahydrate | HCID 21585214 | — |
| Reactant | benzyl 5-oxotetrahydro-2H-pyran-3-ylcarbamate | HCID 25260225 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70981793 | HCID 70981793 | 57% |
Reaction Steps
Benzyl 5-oxotetrahydro-2H-pyran-3-ylcarbamate (4.35 g, 17.45 mmol) and cerium(III) chloride heptahydrate (6.50 g, 17.45 mmol) were dissolved in methanol (100 mL) before cooling to 0° C. Sodium borohydride (0.660 g, 17.45 mmol) was then added slowly. Intense bubbling was observed. The reaction was allowed to stir at 0° C. for 30 min before quenching by addition of acetone (˜3 mL) and stirring at room temperature for 30 additional min. The reaction was then evaporated to dryness. The material was partitioned between DCM and water and the aqueous layer was washed with DCM (5×). The organic layers were combined, dried over sodium sulfate, filtered, and condensed to give impure benzyl 5-hydroxytetrahydro-2H-pyran-3-ylcarbamate (2.5 g, 9.95 mmol, 57.0% yield) as a white solid; 1H NMR (400 MHz, CDCl3) δ ppm 7.28-7.39 (m, 5H), 5.90-6.06 (m, 1H), 5.10 (d, J=4.29 Hz, 2H), 3.59-3.97 (m, 6H), 1.77-2.06 (m, 3H; MS (ESI) m/z 252.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139534B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-3d73b386a90148a8aa8a60a6b0e30a52 |
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| Source note | uspto-grants-2015_09 |
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