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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773086Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 53818101, compound

https://huagongshe.com/reaction/1773086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(S)-(-)-N-Boc-prolinolHCID 643448—
SolventDichloromethaneHCID 6344—
ProductHCID 53818101HCID 53818101—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 2 L, 3-necked round bottomed flask equipped with an overhead stirrer and a N2 inlet was charged with a solution of oxalyl chloride (130 mL, 0.26 mol) in dichloromethane (250 mL). The solution was cooled to −78° C., and a solution of DMSO (20 mL, 0.28 mol) in dichloromethane (30 mL) was added dropwise. After 30 minutes, a solution of (S)—N-Boc-prolinol, Int-7a (40 g, 0.20 mol) in dichloromethane (200 mL) was added dropwise. After 30 minutes, triethylamine (140 mL, 1.00 mol) was added to the solution, and the flask was transferred to an ice/water bath and allowed to stir for another 30 minutes. The reaction mixture was diluted with dichloromethane (200 mL) and washed successively with H2O, 1M HCl, saturated NaHCO3, and brine. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo to provide crude (S)-2-formyl-pyrrolidine-1-carboxylic acid tort-butyl ester, Int-7b (40 g) as oil, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09254292B2
Source datasetuspto-grants-2016_02
ORD IDord-b3a92bc9e2614c71b13f55dc7ad15356
Source noteuspto-grants-2016_02