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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375483Generated: October 30, 2026

Potassium Carbonate → HCID 67745324, compound

https://huagongshe.com/reaction/375483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-Benzyl-1-butoxy-N-[(trimethylsilyl)methyl]methanamineHCID 11097910—
ReactantHCID 67745317HCID 67745317—
CatalystTrifluoroacetic acidHCID 6422—
SolventDichloromethaneHCID 6344—
ProductHCID 67745324HCID 67745324—

Reaction Conditions

Temperature30 °C

Reaction Steps

2 drops of trifluoroacetic acid are added to a solution of 1.3 g of 3,4-dihydro-4,4-diphenyl-2H-thiapyran 1,1-dioxide and 1.75 cm3 of N-butoxymethyl-N-trimethylsilylmethylbenzylamine in 12 cm3 of anhydrous dichloromethane, and the mixture is stirred for 30 minutes at 30° C. 1.75 cm3 of N-butoxymethyl-N-trimethylsilylmethylbenzylamine and 2 drops of trifluoroacetic acid are again added and the mixture is stirred for 2 hours at 35° C. This last procedure is once again repeated and after stirring for 1 hour, 1 g of potassium carbonate is added. The suspension is filtered and the filtrate concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a silica gel column (particle size 0.04-0.06 mm, diameter 3.2 cm, height 35 cm), eluting under a nitrogen pressure of 0.5 bar with a cyclohexane and ethyl acetate mixture (80/20 by volume) and collecting fractions of 30 cm3. Fractions 20 to 28 are pooled and concentrated to dryness under reduced pressure (2.7 kPa). 0.7 g of (4aRS,7aRS)-6-benzyl4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole 1,1-dioxide is obtained in the form of white crystals; melting point 186° l C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484942
Source datasetuspto-grants-1996_01
ORD IDord-8d34b91f51fd4038bd40c558d6ca0711
Source noteuspto-grants-1996_01