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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653456Generated: October 25, 2026

Ethanol → 5,6-Dihydro-4H-thieno[2,3-b]thiopyran-2-sulfonamide 7,7-dioxide

https://huagongshe.com/reaction/653456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant6H-Thieno[2,3-b]thiopyran-2-sulfonamide-7,7-dioxideHCID 13763151—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5,6-Dihydro-4H-thieno[2,3-b]thiopyran-2-sulfonamide 7,7-dioxideHCID 1376315276%

Reaction Steps

A solution of 6H-thieno[2,3-b]thiopyran-2-sulfonamide-7,7-dioxide (3.05 g, 0.011 m) is absolute ethanol (130 ml) and methanol (20 ml) was hydrogenated on a Parr apparatus at 40 psi with 5% palladium on carbon catalyst (250 mg) at ambient temperature. After 15 minutes, 10% palladium on carbon catalyst (350 mg) was added, followed by an identical addition after 30 minutes. After 16 hours, the catalyst was filtered and the filtrate was concentrated in vacuo. The residue was dissolved in absolute ethanol (100 ml) and methanol (50 ml) and hydrogenated at 50 psi with 10% palladium on carbon catalyst (500 mg) for 16 hours. The catalyst was filtered off and the filtrate was evaporated under reduced pressure. The solid residue was chromatographed on silica gel, eluting with 10% methanol-chloroform to give 2.33 g (76%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04677115
Source datasetuspto-grants-1987_06
ORD IDord-23d3e60719b6404c96bb8e7227cfccff
Source noteuspto-grants-1987_06