Potassium Carbonate → 92642-95-0

HRID 1660493ノート

反応式

HRID 1660493 の反応式
Br[CH:2]([CH2:8]Br)[C:3]([O:5]CC)=[O:4].C(=O)([O-])[O-].[K+].[K+].[SH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[OH:23]>CC(C)=O.C(Cl)Cl>[O:23]1[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=2[S:16][CH2:8][CH:2]1[C:3]([OH:5])=[O:4]

参加物

6

実験手順

To a stirred mixture of 41.6 g of ethyl 2,3-dibromopropionate, 400 ml of dry acetone and 11.1 g of potassium carbonate, there was added dropwise at 27° C. a solution of 19.5 g of o-mercaptophenol in 75 ml of acetone. After the addition was complete, the reaction mixture was stirred at room temperature for 10 minutes and an additional 50.9 g of potassium carbonate was added. The reaction mixture then was refluxed for 2 hours, and allowed to stand overnight at room temperature. The mixture was filtered and the solid was washed with acetone, the washings being added to the filtrate. The acetone was stripped to leave a liquid, which was taken up in methylene chloride. The resulting solution was washed with water and dried (MgSO4), and the solvent was stripped. The resulting liquid was dry column chromatographed through silica gel, using a 4:16:80 by volume mixture of tetrahydrofuran, ethyl acetate and hexane (Solvent No. 2) as eluent, to give the ethyl ester of 2,3-dihydro-1,4-benzoxathiin-2-carboxylic acid (1A), as a light yellow liquid, boiling point not determined.

後処理

  1. additionAfter the addition
  2. temperatureThe reaction mixture then was refluxed for 2 hours
  3. waitto stand overnight at room temperature
  4. filtrationThe mixture was filtered
  5. washthe solid was washed with acetone
  6. additionthe washings being added to the filtrate
  7. customto leave a liquid, which
  8. washThe resulting solution was washed with water
  9. dry with materialdried (MgSO4)
  10. customThe resulting liquid was dry column
  11. customchromatographed through silica gel
  12. additionby volume mixture of tetrahydrofuran, ethyl acetate and hexane (Solvent No. 2) as eluent

出典と根拠

ORDレコード
ord-e09ce0a7b8094c7582bb5750a909a707
出典データセット
uspto-grants-1981_12
特許番号
US04308276

反応ノート

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