Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046414Generated: October 27, 2026

Triethylamine → 5-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1046414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,3-Dimethyl-1-butyneHCID 13512—
ReactantEthyl 5-bromothiophene-2-carboxylateHCID 605723—
CatalystCopper iodideHCID 83717—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
Product5-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl esterHCID 5811412897.3%

Reaction Steps

A mixture of 5-bromo-thiophene-2-carboxylic acid ethyl ester (7 g, 30 mmol), copper iodide (1.2 g, 6 mmol), triethylamine (20 mL) in DMF (100 mL) was degassed in a 350 mL pressure bottle. Then tris(dibenzylideneacetone)dipalladium(0) (2.1 g, 3 mmol) and 3,3-dimethyl-but-1-yne (18.3 mL, 150 mmol) were added and heated at 80 degree for 3 hours. The reaction mixture was filtered on celite and washed with ethyl acetate. The solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined and washed with water. After drying and concentration, the crude residue was purified by flash chromatography to yield 6.9 g (95%) of 5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl ester as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569302B2
Source datasetuspto-grants-2013_10
ORD IDord-9d42ed172ece49348d3baaf0d628ad81
Source noteuspto-grants-2013_10