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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442954Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 54256661, compound

https://huagongshe.com/reaction/442954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 53811499HCID 53811499—
SolventDichloromethaneHCID 6344—
ProductHCID 54256661HCID 5425666163.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.), stirred solution of 528 mg (1.44 mmol) of 3-[3-(5-fluoro-2-methylphenylsulfonyloxy)-5-methylphenoxy]propanol, as prepared in the preceding step, 527 μL (3.02 mmol) of N,N-diisopropylethylamine and 307 μL (4.32 mmol) of anhydrous dimethyl sulfoxide in 6.0 mL of anhydrous dichloromethane was added 459 mg (2.88 mmol) of sulfur trioxide pyridine complex. The mixture was warmed to ambient temperature over 30 min and stirred for 16 h. The mixture was then poured into 15 mL of dichloromethane and washed with 5% (w/v) aqueous citric acid (2×25 mL). Each wash was extracted with 5 mL of dichloromethane and the combined extracts were washed with brine (25 mL), dried over Na2SO4 and concentrated. The resulting material was chromatographed on 35 g of silica gel with dichloromethane followed by 3% ethyl acetate-dichloromethane to afford 320 mg (61%) of the title compound as a colorless syrup: Mass spectrum (MALDI-TOF, α-cyano-4-hydroxycinnamic acid matrix) calcd. for C17H17FO5S: 375.1 (M+Na). Found: 375.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891909
Source datasetuspto-grants-1999_04
ORD IDord-835f811b5b0a49bfbf5c5708e057345f
Source noteuspto-grants-1999_04