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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108340Generated: October 30, 2026

Acetic Anhydride → HCID 12043500, compound

https://huagongshe.com/reaction/1108340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 18388323HCID 18388323—
CatalystHCID 178418390HCID 178418390—
SolventAcetic AcidHCID 176—
ProductHCID 12043500HCID 1204350077.8%

Reaction Steps

A mixture of ethyl 5-azido-4,5,6,7-tetrahydro-3-isopropylthio-4-oxobenzo[c]thiophene-1-carboxylate (1.60 g), palladium-carbon (5%, 50% wet, 1.6 g), acetic acid (30 ml) and acetic anhydride (15 ml) was subjected to a catalytic reduction reaction at room temperature under 1 atm. The insoluble substances were filtered off; the filtrate was poured over water and extracted with ethyl acetate. The organic layer was washed with water, a saturated aqueous solution of sodium hydrogen carbonate and water in that order, and dried (MgSO4), after which the solvent was distilled off to yield ethyl 5-acetylamino-4,5,6,7-tetrahydro-3-isopropylthio-4-oxobenzo[c]thiophene-1-carboxylate (1.30 g, 77.8%), which was then recrystallized from ethyl acetate-hexane. Colorless prisms. Melting point 170-171° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066658
Source datasetuspto-grants-2000_05
ORD IDord-290e1b25b2e44d5292e6cfd7ac7bd170
Source noteuspto-grants-2000_05