HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357625Generated: November 2, 2026
Sodium borohydride → HCID 68455343, compound
https://huagongshe.com/reaction/2357625
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86607614 | HCID 86607614 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68455343 | HCID 68455343 | — |
Reaction Steps
(R)-allyl 2-(isopropylcarbamoyl)-5-methylpyrrolidine-1-carboxylate (450 mg, 1769 μmol) was dissolved in acetonitrile (13 mL) before sodium borohydride (268 mg, 7078 μmol) and tetrakis(triphenylphosphine)palladium(0) (102 mg, 88 μmol) were added at ambient. The reaction mixture was heated to 50° C. for 4 h then filtered through a pad of silica gel and washed with chloroform to remove impurities. The silica was washed again with methanol to obtain the title compound as a mixture of diastereomers (˜60:40). MS (ES+): 171(M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759337B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-886493d56fc444ea9026b0e69b50dec6 |
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| Source note | uspto-grants-2010_07 |
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