Ethyl bromoacetate → HCID 13289995, compound

HRID 485846Notes

Reaction equation

HRID 485846 reaction equation
[Cl:1][C:2]1[C:3]([OH:18])=[CH:4][C:5]2[C:9]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:8][S:7][C:6]=2[C:16]=1[Cl:17].Br[CH2:20][C:21]([O:23]CC)=[O:22].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[Cl:1][C:2]1[C:3]([O:18][CH2:20][C:21]([OH:23])=[O:22])=[CH:4][C:5]2[C:9]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:8][S:7][C:6]=2[C:16]=1[Cl:17]

Participants

5

Procedure

A mixture of 2.7 g of 6,7-dichloro-5-hydroxy-3-phenylbenzo[b]thiophene, 1.6 g of ethyl bromoacetate, 1.3 g of potassium carbonate and 30 ml of dimethylformamide is stirred at 60°-70° for 30 min. The mixture is filtered to remove inorganic salts and the filtrate is concentrated in vacuo to an oily residue. To the residue is added 10 mil of 40% sodium hydroxide and 30 ml of water and the mixture was heated on a steam bath for 30 min. After acidification of the mixture to pH 2, the solid product was extracted into ether, washed and dried. Concentration in vacuo gives 2.6 g of [(6,7-dichloro-3-phenylbenzo[b]thien-5-yl)oxy]acetic acid as crystals which have mp 152°-154° after recrystallization from acetone-hexane.

Workup

  1. filtrationThe mixture is filtered
  2. customto remove inorganic salts
  3. concentrationthe filtrate is concentrated in vacuo to an oily residue
  4. additionTo the residue is added 10 mil of 40% sodium hydroxide and 30 ml of water
  5. temperaturethe mixture was heated on a steam bath for 30 min
  6. extractionAfter acidification of the mixture to pH 2, the solid product was extracted into ether
  7. washwashed
  8. customdried
  9. concentrationConcentration in vacuo

Sources & evidence

ORD record
ord-d24b7b7e1c484fe09720d0f7bc7e0348
Source dataset
uspto-grants-1985_08
Patent number
US04537976

Reaction notes

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