HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202581Generated: November 3, 2026
4-Benzhydryloxypiperidine → HCID 86680286, compound
https://huagongshe.com/reaction/2202581
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Benzhydryloxypiperidine | HCID 3017584 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86680287 | HCID 86680287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86680286 | HCID 86680286 | — |
Reaction Steps
Into a 100-mL three-neck flask, 1.1 g (4.0 mmol) of 4-benzhydryloxypiperidine synthesized in Production Example 1, 1.0 g (4.0 mmol) of methyl N-tert-butoxycarbonyl-5-formylpyrrole-2-carboxylate, and 20 mL of dichloromethane were fed under an argon atmosphere, and the internal temperature was cooled to 0° C. Thereinto, 1.3 g (6.1 mmol, 1.5 eq.) of sodium triacetoxyborohydride was added at an internal temperature of not higher than −5° C., and the mixture was stirred for 5 minutes at the same temperature. Then, the mixture was heated to a room temperature and stirred overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365553B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-5613559267fa4be1818c30749056768c |
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| Source note | uspto-grants-2016_06 |
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