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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382365Generated: November 1, 2026

Methyl thieno[2,3-b]thiophene-2-carboxylate → Thieno[2,3-b]thiophene-2-methanol

https://huagongshe.com/reaction/1382365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl thieno[2,3-b]thiophene-2-carboxylateHCID 12475296—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
ProductThieno[2,3-b]thiophene-2-methanolHCID 14460451—

Reaction Steps

A solution of methyl thieno[2,3-b]thiophene-2-carboxylate (19.8 g. 0.1 mol) in dry ether (75 mL) was added at a rapid drip rate (1 hour, 45 minutes) to a suspension of lithium aluminum hydride (7.59 g, 0.2 mol) in ether (500 mL) cooled in an ice-water bath. During the addition, precipitated material on the inside of the flask was kept suspended in the reaction medium. After the addition was complete stirring was continued at room temperature for 3 hours. The reaction mixture was cooled in an ice-water bath and there was added in succession, slowly, dropwise with vigorous stirring: water (7.6 ml); 20% aqueous NaOH (22.8 mL); water (7.6 mL); water (4 mL); 20sodium hydroxide (12 mL); water (4 ml). Vigorous stirring was continued until a granular precipitate was obtained. The ether was decanted and the solids were washed by decantation three times with ether. The combined ether fractions were dried (MgSO4), filtered, and evaporated in vacuo to leave 16.33 g of white, solid 2-hydroxymethylthieno[2,3-b]thiophene, m.p. 85°-87° C. Recrystallization from hexane gave material with m.p. 86°-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04806562
Source datasetuspto-grants-1989_02
ORD IDord-38eb995f81cc400280065aaa6a27b42e
Source noteuspto-grants-1989_02