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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973419Generated: November 1, 2026

Ethanol → HCID 12428607, compound

https://huagongshe.com/reaction/1973419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantIodoethaneHCID 6340—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178469712HCID 178469712—
SolventWaterHCID 962—
ProductHCID 12428607HCID 12428607—

Reaction Steps

A mixture of 1.38 parts of ethyl 4-hydroxy-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridine-3-carboxylate, 11 parts by volume of 10 percent aqueous potassium hydroxide, 44 parts by volume of ethanol and 45 parts by volume of water and 1.5 parts by volume of ethyl iodide is refluxed for 4 hours and the product is isolated in a manner similar to that described in Example 13, whereby 1-ethyl-1,4,5,6,7,8-hexahydro-4-oxo[1]benzothieno[2,3-b]pyridine-3-carboxylic acid is obtained as crystals. Recrystallization from ethanol and, then, from tetrahydrofuran gives colorless needles melting at 218°-221° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03997545
Source datasetuspto-grants-1976_12
ORD IDord-60a4c8b767c547efa676ef969e9731c8
Source noteuspto-grants-1976_12