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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675540Generated: October 30, 2026

Triethylamine → HCID 178499327, compound

https://huagongshe.com/reaction/1675540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,3-Dimethyl-1-butyneHCID 13512—
ReactantHCID 178499356HCID 178499356—
CatalystCopper iodideHCID 83717—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventDimethylformamideHCID 6228—
ProductHCID 178499327HCID 178499327—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a 25 mL RBF under nitrogen, 3-[(1,4-dioxa-spiro[4.5]dec-8-yl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-5-iodo-thiophene-2-carboxylic acid methyl ester (1 eq.), copper iodide (0.025 eq.) and tris(dibenzylideneacetone) dipalladium (0) (0.01 eq.) are taken. DMF, triethylamine (2.5 eq.) and 3,3-dimethyl-but-1-yne (2 eq.) are added and the reaction mixture is stirred at 40° C. for 2 h under a N2 atmosphere. The reaction mixture is filtered on celite and washed with ethyl acetate. The solution is diluted with water and extracted 2 times with ethyl acetate. The organic phases are combined and washed 3 times with water. The organic layer is separated, dried (Na2SO4), evaporated to about 2 mL and then 8 mL of heptane is added. It is evaporated to 2-4 mL and cooled in an ice bath. The formed white solid is filtered, washed with heptane and dried in oven to obtain 5-(3,3-dimethyl-but-1-ynyl)-3-[(1,4-dioxa-spiro[4.5]dec-8-yl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003685B2
Source datasetuspto-grants-2011_08
ORD IDord-c6d9aaa10ef445edb4dc92743ed645ba
Source noteuspto-grants-2011_08