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

HRID 39291
Notes
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Reaction equation

HRID 39291 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[S:7][C:8](Br)=[CH:9][CH:10]=1)=[O:5])[CH3:2].C(N(CC)CC)C.[CH3:19][C:20]([CH3:24])([CH3:23])[C:21]#[CH:22]>CN(C=O)C.[Cu](I)I.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[CH2:1]([O:3][C:4]([C:6]1[S:7][C:8]([C:22]#[C:21][C:20]([CH3:24])([CH3:23])[CH3:19])=[CH:9][CH:10]=1)=[O:5])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

HCID 8471TriethylamineHCID 135123,3-Dimethyl-1-butyneHCID 605723Ethyl 5-bromothiophene-2-carboxylate

Product 1

HCID 581141285-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl esterYield 97.3%

Reagents, catalysts & solvents 3

HCID 83717Copper iodideCatalyst
HCID 9811564
Bis(dibenzylideneacetone)palladium
Catalyst
HCID 6228DimethylformamideSolvent

Procedure

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.

Workup

  1. customwas degassed in a 350 mL pressure bottle
  2. temperatureheated at 80 degree for 3 hours
  3. filtrationThe reaction mixture was filtered on celite
  4. washwashed with ethyl acetate
  5. additionThe solution was diluted with water
  6. extractionextracted twice with ethyl acetate
  7. washwashed with water
  8. customAfter drying
  9. concentrationconcentration
  10. customthe crude residue was purified by flash chromatography

Sources & evidence

ORD record
ord-32d5be6c632a4182b5049936e8f684b9
Source dataset
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08524764B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes