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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458182Generated: November 1, 2026

Dimethyl Sulfoxide → 1,1,1-Trifluoro-3-[(N-acetylprolyl)alanylprolylamino]-butane-2,2-diol

https://huagongshe.com/reaction/1458182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1,1,1-Trifluoro-3-[(N-acetylprolyl)alanylprolylamino]butan-2-olHCID 14503266—
SolventDichloromethaneHCID 6344—
Product1,1,1-Trifluoro-3-[(N-acetylprolyl)alanylprolylamino]-butane-2,2-diolHCID 53770514—

Reaction Steps

To a solution of oxalyl chloride (72 μl, 0.83 mmol) in methylene chloride (1 ml) under an argon atmosphere and cooled in a dry ice-acetone bath was added dimethylsulfoxide (0.12 ml, 1.65 mmol) with stirring. After 5 minutes, a solution of the compound of example 57 (0.25 g, 0.55 mmol) in methylene chloride (1.5 ml) was added. The reaction mixture was stirred for 15 minutes, triethylamine (0.50 ml,3.58 mmol) then added and the reaction warmed to room temperature for 30 minutes. The reaction mixture was placed directly onto a silica gel column and eluted with methylene chloride-methanol. Trituration of the resultant oily solid with ether-hexane and filtration gave the above-named product, (50 mg, 0.11 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849866
Source datasetuspto-grants-1998_12
ORD IDord-7b21a6534ee34fdc9aa278ce119014f1
Source noteuspto-grants-1998_12