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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605970Generated: October 30, 2026

Ethanol → HCID 12428607, compound

https://huagongshe.com/reaction/1605970

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 % 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. Recrytallization from ethanol and, then, from tetrahydrofuran gives colorless needles melting at 218°-221°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03951989
Source datasetuspto-grants-1976_04
ORD IDord-6eb5b8aff02140328c45c5a375156924
Source noteuspto-grants-1976_04