HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222247Generated: October 30, 2026
Dichloromethane → HCID 67108955, compound
https://huagongshe.com/reaction/222247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Benzyl carbazate | HCID 79242 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67108955 | HCID 67108955 | 57% |
Reaction Steps
To a mixture of tert-butyl 4-oxopiperidine-1-carboxylate (10.0 g), benzylhydrazinecarboxylate (16.7 g), DCM (150 mL), and acetic acid (5.75 mL) was added sodium triacetoxyborohydride (31.9 g), followed by stirring at room temperature for 2.5 days. To the reaction liquid was added water, and the organic phase was separated. The aqueous phase was extracted with chloroform, and the combined organic phase was washed with water, a saturated aqueous sodium bicarbonate, and saturated brine in this order, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=100/0 to 90/10) to obtain tert-butyl 4-{2-[(benzyloxy)carbonyl]hydrazino}piperidine-1-carboxylate (10.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207199B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-da855ba55dc94d989a6553767eb3dc31 |
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| Source note | uspto-grants-2012_06 |
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