Methyl Ethyl Ketone → HCID 13985633, compound

HRID 652650Notes

Reaction equation

HRID 652650 reaction equation
[Cl:1][C:2]1[C:7]2[S:8][CH:9]=[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[F:17])[C:6]=2[CH:5]=[CH:4][C:3]=1[OH:18].Br[CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22].CC(=O)CC.C(=O)([O-])[O-].[K+].[K+]>C(Cl)Cl.CN(C)C=O>[CH2:24]([O:23][C:21](=[O:22])[CH2:20][O:18][C:3]1[CH:4]=[CH:5][C:6]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[F:17])=[CH:9][S:8][C:7]=2[C:2]=1[Cl:1])[CH3:25]

Participants

7

Reactant 4

HCID 6569Methyl Ethyl KetoneHCID 7748Ethyl bromoacetateHCID 11430Potassium CarbonateHCID 13985632HCID 13985632, compound

Product 1

HCID 13985633HCID 13985633, compoundYield 78.2%

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolventHCID 6344DichloromethaneSolvent

Procedure

A mixture of 8.3 g of 7-chloro-6-hydroxy-3-(2-fluorophenyl)benzo[b]thiophene, 6.0 g of ethyl bromoacetate, 60 ml of 2-butanone, 5 ml of dimethylformamide and 4 g of potassium carbonate is heated under reflux until the standing material completely dissovles. Methylene chloride is added to the cooled reaction mixture and the resultant precipitate is collected. Evaporation of the filtrate gives 8.5 g of ethyl{[7-chloro-3-(2-fluorophenyl)benzo[b]thien-6-yl]oxy}acetate.

Workup

  1. temperatureis heated
  2. temperatureunder reflux until the standing material
  3. customthe resultant precipitate is collected
  4. customEvaporation of the filtrate

Sources & evidence

ORD record
ord-3429aaeef8fe4a058657bb450bd73602
Source dataset
uspto-grants-1987_06
Patent number
US04672138

Reaction notes

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