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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098352Generated: October 30, 2026

Dimethyl Sulfoxide → Methyl 4-formylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1098352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantMethyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 45123042—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-formylpiperidine-1-carboxylateHCID 4512304178%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of oxalyl chloride (4.1 mL, 8.2 mmol) in dichloromethane (4 mL) at −78° C. was added dropwise a solution of dimethylsulfoxide (1.2 mL, 16.4 mmol) in dichloromethane (4 mL). After stirring for 5 min, a solution of 4-hydroxymethyl-piperidine-1-carboxylic acid methyl ester (1.3 g, 7.5 mmol) in dichloromethane (5 mL) was added. The resulting solution was stirred for another 5 min, then triethylamine (5.2 mL, 37.3 mmol) was added and the mixture allowed to warm to −10° C. After stirring for 1 h, dichloromethane (100 mL) was added, and the organic layer was washed with 1M aqueous phosphoric acid, 1M aqueous sodium hydroxide, and brine. The solution was dried over sodium sulfate then evaporated to afford the title intermediate as a wheat colored oil (1.0 g, 5.8 mmol, 78%). 1H NMR (300 MHz, DMSO-d6): δ (ppm) 1.36 (m, 2H), 1.83 (m, 2H), 2.48 (br m, 1H), 2.93 (br t, 2H), 3.56 (s, 3H), 3.80 (br d, 2H), 9.56 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143279B2
Source datasetuspto-grants-2012_03
ORD IDord-a4a6b0167e2349cab102b2401a0997f6
Source noteuspto-grants-2012_03