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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330000Generated: October 29, 2026

1,5-Diazabicyclo(4.3.0)non-5-ene → Methyl thieno[2,3-b]thiophene-2-carboxylate

https://huagongshe.com/reaction/330000

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-Diazabicyclo(4.3.0)non-5-eneHCID 76349—
ReactantMethyl 2-(3-formyl-2-thienylthio)acetateHCID 11959090—
SolventMethanolHCID 887—
ProductMethyl thieno[2,3-b]thiophene-2-carboxylateHCID 1247529680.6%

Reaction Steps

To a solution of methyl (3-formylthiophene-2-ylthio)acetate (19.31 g, 91 mmol) in methanol (150 mL) was added 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) (1 mL, 1 g, 8.05 mmol) and the stirred reaction flask was immediately immersed in an ice-water bath. Stirring was continued for 30 minutes and the mixture was filtered to give a tacky solid product which was washed with a little cold (-20° C.) methanol. The solvent was evaporated in vacuo from the mother liquor and the residue was partitioned between ether and aqueous sodium bicarbonate. The water layer was washed with ether twice, and the combined ether extracts were dried (MgSO4), filtered, and the solvent evaporated in vacuo to give an oil which solidified when triturated with a little cold (-20° C.) methanol. This was combined with the original solid product to give a total of 14.55 g of methyl thieno-[2,3-b]thiophene-2-carboxylate, m.p. 101°-105° C. Recrystallization from methanol gave product with m.p. 106°-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04894390
Source datasetuspto-grants-1990_01
ORD IDord-8a08183c232648dcae4a1418a8413387
Source noteuspto-grants-1990_01