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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291933Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 21278431, compound

https://huagongshe.com/reaction/2291933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 21278488HCID 21278488—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 21278431HCID 21278431—

Reaction Conditions

Temperature-60 °C

Reaction Steps

18 ml of a molar solution of dimethylsulfoxide in methylene chloride were introduced dropwise at -60° C. into 9.5 ml of a molar solution of oxalyl chloride in methylene chloride and the mixture was stirred at -60° C. for 5 minutes. Then, at -60° C., a solution of 724 g of 4-hydroxy-methyl-1-(2-propynyl)-1H-pyrrole-3-carbonitrile was added dropwise and the mixture was stirred at -60° C. for 5 hours, after which, still at -60° C., 25 ml of a molar solution of triethylamine in methylene chloride were added dropwise. The mixture was stirred at -60° C. for 30 minutes and the reaction mixture was allowed to return to ambient temperature. Water was added and the mixture was stirred and decanted. The organic phase was washed with a saturated aqueous solution of sodium chloride and concentrated to dryness by distilling under reduced pressure. The residue was chromatographed over silica and was eluted with a mixture of hexane and ethyl acetate (1-1) to obtain 702 mg of 4-formyl-1-(2-propynyl)-1H-pyrrol-3-carbonitrile melting at 114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04798901
Source datasetuspto-grants-1989_01
ORD IDord-dd03fa13673d4c079f46debcab1a21bc
Source noteuspto-grants-1989_01