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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975474Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 19099323, compound

https://huagongshe.com/reaction/1975474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 19099247HCID 19099247—
SolventDichloromethaneHCID 6344—
ProductHCID 19099323HCID 190993239.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of oxalyl chloride (23 ml) in dichloromethane was added dropwise dimethyl sulfoxide (374 ml) while keeping the temperature below -50° C. After the mixture was stirred for 30 minutes at -50° C.~-60° C., 1.2-bis(benzyloxycarbonyl)-4-(1-hydroxyethyl)pyrazolidine (675 g) was added dropwise below -50° C. After the mixture was stirred for 45 minutes at -50° C.~-60° C., triethylamine (122 ml) was added dropwise below -50° C. The reaction mixture was allowed to warm to 0° C. and quenched with water (500 ml). The aqueous layer was separated and extracted twice with dichloromethane (200 ml×2). The combined organic layer was washed with 1N hydrochloric acid (200 ml×2), saturated sodium bicarbonte (200 ml), and 5% sodium chloride (200 ml), dried over magnesium sulfate, and evaporated under reduced pressure. The residue was chromatographed on silica gel (820 ml, hexane:ethyl acetate=2:1~1:1) to give 1,2-bis(benzyloxycarbonyl)pyrazolidin-4-yl methyl ketone (61.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05286721
Source datasetuspto-grants-1994_02
ORD IDord-001b5da0991448ed86e080fad5263e4f
Source noteuspto-grants-1994_02