HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407788Generated: November 2, 2026
Sodium triacetoxyborohydride → HCID 58504055, compound
https://huagongshe.com/reaction/2407788
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Benzyl (3-Oxopropyl)carbamate | HCID 10398106 | — |
| Reactant | HCID 58504081 | HCID 58504081 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58504055 | HCID 58504055 | 87.8% |
Reaction Steps
The compound prepared in Example 302 (0.455 g) was suspended in 1,2-dichloroethane (10 mL). Benzyl 3-oxopropylcarbamate (0.425 g) and beaded molecular sieves were added and the reaction mixture stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.870 g) was added and the reaction mixture stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium bicarbonate solution and brine. The organics were dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford the crude material, which was purified by flash column chromatography (eluant: 20-30% ethyl acetate/hexane) to furnish the title compound (0.629 g) with the following physical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809538B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-debe572ce94e4d25817d5a2c75685a3b |
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| Source note | uspto-grants-2014_08 |
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