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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388265Generated: November 1, 2026

3,3-Dimethyl-1-butyne → HCID 178499344, compound

https://huagongshe.com/reaction/2388265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-Dimethyl-1-butyneHCID 13512—
ReactantHCID 178499257HCID 178499257—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 178499344HCID 178499344—

Reaction Steps

To a solution of compounds 5-bromo-3-[(trans-4-hydroxy-cyclohexyl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester (500 mg, 1.09 mmol) and 3,3-Dimethyl-but-1-yne (385 mg, 4.69 mmol) in DMF (0.5 mL), triethylamine (1.06 mL) and tris(dibenzylideneacetone)dipalladium (0) (70 mg, 0.08 mmol) are added and the reaction mixture is stirred under reflux conditions for 16 h under a N2 atmosphere. DMF and triethylamine are removed under reduced pressure and the residue is partitioned between water and ethyl acetate. The organic layer is separated, dried (Na2SO4), concentrated and the residue is purified by column chromatography using ethyl acetate and hexane (1:2) as eluent to obtain 5-(3,3-dimethyl-but-1-ynyl)-3-[(trans-4-hydroxy-cyclohexyl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester as a solid, 330 mg (66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269014B2
Source datasetuspto-grants-2012_09
ORD IDord-ecdd876aea4b4e188786e72b9f561071
Source noteuspto-grants-2012_09