HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158511Generated: November 3, 2026
Sodium triacetoxyborohydride → HCID 68676597, compound
https://huagongshe.com/reaction/1158511
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | [N-(methoxycarbony)-L-tert-leucinyl]hydrazine | HCID 10679660 | — |
| Reactant | HCID 44819177 | HCID 44819177 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68676597 | HCID 68676597 | — |
Reaction Steps
(S)-3-Benzyl-4-((3aS,8aR)-2,2-dimethyl-8,8a-dihydro-3 aH-indeno[1,2-d]oxazol-3-yl)-3-hydroxy-4-oxo-butyraldehyde (21h) (0.082 g, 0.21 mmol) and [N-(methoxycarbony)-L-tert-leucinyl]hydrazine (0.048 g, 0.23 mmol, prepared as reported JMC, 41, 3387, 1998) in dry THF (10 mL) was stirred for 3 h and [the LCMS (ESI+) shows 565 (M+)], then Na(OAc)3BH (0.137 g, 0.64 mmol) was added and stirred overnight. The reaction mixture was quenched with water and evaporated. The residue was dissolved in dichloromethane and washed with water, brine and dried. The crude product was analysed by LCMS (ESI+) which showed 567 (M+) the title compound with a minor quantity of the compound lacking the protection group on the indanol moiety [MS (ESI+): 527 (M+)]. This mixture was alkylated by the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807677B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-c9fb87735e8542d8873517f02b2081a3 |
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| Source note | uspto-grants-2010_10 |
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