HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39700Generated: October 26, 2026
4-Benzyloxycarbonylamino-4-hydroxymethyl piperidine-1-carboxylic acid tert-butyl ester → tert-Butyl 4-amino-4-(hydroxymethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/39700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Benzyloxycarbonylamino-4-hydroxymethyl piperidine-1-carboxylic acid tert-butyl ester | HCID 66741770 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 4-amino-4-(hydroxymethyl)piperidine-1-carboxylate | HCID 22975819 | — |
Reaction Steps
To 10 mL of an ethanol solution containing 0.55 g of tert-butyl 4-(((benzyloxy)carbonyl)amino)-4-(hydroxymethyl)piperidine-1-carboxylate, 0.10 g of 20% palladium hydroxide-carbon was added at room temperature, and the mixture was stirred at 40° C. for 3 hours under a hydrogen atmosphere. The insoluble material filtered off, and the filtration residue thus obtained was washed 3 times with chloroform. The filtrate and the washing solution were combined, and the solvent was removed under reduced pressure to obtain 0.39 g of a dark brown oily substance, tert-butyl 4-amino-4-(hydroxymethyl)piperidine-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08524738B2 |
|---|
| Source dataset | uspto-grants-2013_09 |
|---|
| ORD ID | ord-c24a0a827f9e4dfc85ef3b68c16bd8a9 |
|---|
| Source note | uspto-grants-2013_09 |
|---|