Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634742Generated: November 1, 2026

Benzyl 4-(hydroxymethyl)piperidine-1-carboxylate → Benzyl 4-formylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1634742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 736490—
ReactantHCID 178418287HCID 178418287—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-formylpiperidine-1-carboxylateHCID 277627293%

Reaction Steps

An ice cold solution of N-benzyloxycarbonyl-4-hydroxymethylpiperidine (2.5 g, 10 mmol) in 100 mL CH2Cl2 is treated with pyridinium chlorochromate (3.23 g, 15 mmol). The reaction is stirred at ambient temperature for 3 hours. The mixture was diluted with 100 mL Et2O and filtered through a plug of silica. The filtrate was concentrated in vacuo to provide 2.3 g of the title compound as a pale green liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506901B2
Source datasetuspto-grants-2003_01
ORD IDord-ad3b20eb3196434582f8384b52afc9f5
Source noteuspto-grants-2003_01