HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402085Generated: October 26, 2026
Benzyl chloroformate → HCID 58745550, compound
https://huagongshe.com/reaction/402085
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | rac-tert-butyl (3R,4R)-4-amino-3-hydroxypiperidine-1-carboxylate | HCID 10727458 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58745550 | HCID 58745550 | — |
Reaction Steps
To a stirred solution of (±)-trans-4-amino-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (9.48 mmol, 2.05 g) in a biphasic mixture of DCM (10 mL) and saturated sodium bicarbonate (10 mL) at 0° C. was added benzyl chloroformate (2.0 mL) drop-wise and continued stirring at 0-5° C. for 1 h. The organic layer was separated, and the aqueous layer was extracted with DCM. The combined organic layers were dried, filtered and concentrated under reduced pressure. The residue was purified by flash silica gel column chromatography by eluting with 50% ethyl acetate in hexanes to provide (±)-trans-4-benzyloxycarbonylamino-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741900B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-c4bfb5e188a34eb5974b7734bba8348b |
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| Source note | uspto-grants-2014_06 |
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