HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533967Generated: October 30, 2026
Sodium borohydride → HCID 58033108, compound
https://huagongshe.com/reaction/533967
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 58033030 | HCID 58033030 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58033108 | HCID 58033108 | 45.3% |
Reaction Steps
N-[5-(2-Chloro-benzoyl)-thiazol-2-yl]-2-phenyl-butyramide (102 mg, 0.265 mmol) was suspended in 1 mL of anhydrous methanol. Sodium borohydride (30.3 mg, 0.801 mmol) was slowly added and the resulting pale yellow solution was allowed to stir for 1 hour at room temperature. After stirring for one hour a second aliquot of sodium borohydride (30.3 mg, 0.801 mmol) was added. The reaction mixture was allowed to stir for an additional hour and then the crude product was evaporated to dryness and then dissolved in a minimum of ethyl acetate. The organic layer was washed three times with an equal volume of 1N hydrochloric acid, saturated aqueous sodium bicarbonate, and saturated aqueous sodium chloride. The organic layer was then dried over sodium sulfate, filtered, and evaporated to dryness. The crude product was further purified by reverse-phase preparative liquid chromatography to yield the pure product (46 mg, 0.12 mmol, 45%) ESI-MS m/z calc. 386.1. found 387.3 (M+1)+ Retention time 3.83 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853415B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-185dea4c86e34de890a6d6a57e5c7b8b |
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| Source note | uspto-grants-2014_10 |
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