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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033081Generated: November 1, 2026

Ethylamine → HCID 86747813, compound

https://huagongshe.com/reaction/1033081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 67692704HCID 67692704—
SolventPyridineHCID 1049—
ProductHCID 86747813HCID 86747813—

Reaction Conditions

Temperature-10 °C

Reaction Steps

5,6-Dihydro-6-ethoxymethyl-4-hydroxy-4H-thieno[2,3-b]thiopyran-2-sulfonamide-7,7-dioxide (4.25 g, 0.0123 mol) was dissolved in dry pyridine (25 ml) and the solution was cooled to -10° C. p-Toluenesulfonyl chloride (5.14 g, 0.027 mol) was added and the mixture was stirred at -10° C. for 5 hours. Anhydrous ethylamine (26 ml, 0.4 mol) was added and the mixture was stirred for 2 hours at room temperature. Finally, 70% ethylamine (32 ml. 0.40 mol) was added and the mixture was heated at 50° C. overnight. The dark mixture was concentrated in vacuo and the residual oil was taken up in ethyl acetate (100 ml) and saturated sodium bicarbonate (100 ml). The aqueous layer was separated and extracted with ethyl acetate. The combined ethyl, acetate solutions were washed with saturated sodium chloride, dried, filtered and concentrated in vacuo. The oil obtained was a 2:1 mixture of cis and trans isomers which were separated by silica gel chromatography using 7.5% methanol-chloroform. Total recovery was 2.43 g. Yield of 33 was 54%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308863
Source datasetuspto-grants-1994_05
ORD IDord-5671a578672c475ab5551ad987a853fd
Source noteuspto-grants-1994_05