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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479783Generated: October 30, 2026

tert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylate → 1-Boc-piperidine-3-carboxaldehyde

https://huagongshe.com/reaction/479783

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2763851—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product1-Boc-piperidine-3-carboxaldehydeHCID 996444880%

Reaction Steps

To a stirred suspension of pyridinium chlorochromate (98%, 34.0 g, 0.155 mol) and Celite (24 g) in 200 mL of dry CH2Cl2 was added N-Boc-3-piperidinemethanol (2) (22.15 g, 0.103 mol) in 30 mL of CH2Cl2 in one portion, and the mixture was stirred at room temperature overnight. The mixture was filtered by passing through a funnel filled with 20 g of Celite. After the solvent was removed, the remaining oily residue was purified by a flash column (silica gel; hexane:ethyl acetate, 4:1) to afford 3 as a colorless oil 17.5 g (80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645980B1
Source datasetuspto-grants-2003_11
ORD IDord-d9fff792ad9d416eaeb6419be4da1fba
Source noteuspto-grants-2003_11