HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375093Generated: November 3, 2026
Sodium borohydride → HCID 69417629, compound
https://huagongshe.com/reaction/1375093
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86590648 | HCID 86590648 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69417629 | HCID 69417629 | 100.3% |
Reaction Steps
A stirred suspension of [1-(4-{(benzotriazol-1-ylmethyl)-amino}-phenyl)-cyclopentyl]-acetic acid tert-butyl ester (0.21 g) in ethanol (10 mL), under argon, was treated with sodium borohydride (0.051 g). After stirring at room temperature for 2 hours a further aliquot of sodium borohydride (0.017 g) was added and stirring was continued for a further hour, then a further aliquot of sodium borohydride (0.017 g) was added and stirring was continued for a further hour. The reaction mixture was then evaporated and the residue was treated with water (15 mL) and ethyl acetate (25 mL). The organic phase was separated and then washed with water (15 mL), then with brine (15 mL), then dried over magnesium sulfate and then evaporated to give the title compound (0.15 g) as an amber oil which crystallised on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166616B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-4f0d6d84fe434e1cad382bd17dcbb38a |
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| Source note | uspto-grants-2007_01 |
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