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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419345Generated: October 30, 2026

Dimethyl Sulfoxide → tert-Butyl 4-formylpiperidine-1-carboxylate

https://huagongshe.com/reaction/419345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
ReactantTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—

Reaction Steps

Oxalyl chloride (18.5 mL, 2M in DCM, 37.0 mmol) in DCM (230 mL) was cooled with a dry ice/acetone bath. DMSO (5.15 mL, 72.6 mmol) was added dropwise via addition funnel and the reaction was stirred for 10 min. N-Boc-4-piperidinemethanol in DCM (20 mL) was added dropwise via addition funnel and the reaction was stirred for 15 min. TEA (17.0 mL, 122 mmol) was then added dropwise via addition funnel and the reaction was warmed to rt. The reaction was diluted with diethyl ether, washed with H2O and brine, dried (MgSO4) and concentrated to provide the title compound (5.36 g, 25.1 mmol, 100%, approximately 96% pure, used without further purification). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.29-1.34 (m, 3H), 1.37 (s, 9H), 1.75-1.83 (m, 2H), 2.87 (s, 2H), 3.78 (d, J=13.2 Hz, 2H), 9.56 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-c913435c46a241ed875f145881d81b61
Source noteuspto-grants-2012_01