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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904761Generated: November 2, 2026

Sodium Hydroxide → 4-methyl-6H,7H-thieno[3,2-c]pyridine

https://huagongshe.com/reaction/1904761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-(2-Thiophen-2-yl-ethyl)-acetamideHCID 21821173—
SolventBenzeneHCID 241—
Product4-methyl-6H,7H-thieno[3,2-c]pyridineHCID 21821177—

Reaction Steps

To 5.70 g (0.0337 mol) of 2-acetylaminoethylthiophene (f-l) was added 157 ml of dry benzene; and while being refluxed, a mixture of 13.80 g (0.09 mol) of phosphorus oxychloride and 63 ml of dry benzene was added dropwise to the solution. After being refluxed for 2 hr., the mixture was cooled with ice, and the reaction solution was poured into 315 g of ice. Under ice-cooling, the mixture was adjusted to pH 10 or more with 48% aqueous NaOH, and the solution was extracted with ether. After being washed with saturated brine, the ether layer was dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure to give 4.45 g (Yield : 87.3%) of the objective product, 4-methyl-6, 7-dihydrothieno[3, 2-c]pyridine (g-l) as dark red liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839365
Source datasetuspto-grants-1989_06
ORD IDord-29007c3f6af24a5bbf723fd51d0f8d65
Source noteuspto-grants-1989_06