2-Methyl-2-butene → 5-(4-Chlorophenylthio)thiophene-2-carboxylic acid

HRID 412007ノート

反応式

HRID 412007 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[S:13][C:12]([CH:14]=[O:15])=[CH:11][CH:10]=2)=[CH:4][CH:3]=1.CC(=CC)C.[OH:21]P([O-])(O)=O.[K+].[O-]Cl=O.[Na+].OS([O-])(=O)=O.[K+]>C1COCC1.CC(O)(C)C.O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:8][C:9]2[S:13][C:12]([C:14]([OH:21])=[O:15])=[CH:11][CH:10]=2)=[CH:6][CH:7]=1

参加物

9

実験手順

5-(4-Chlorophenylsulfanyl)thiophene-2-carboxaldehyde (6.1 g, 24 mmol) is dissolved in a mixture of THF, tBuOH, and water (3:3:1, 255 mL). 2-methyl-2-butene (20.3 mL, 192 mmol) is added followed by KH2PO4 (9.8 g, 72 mmol) and then NaClO2 (80%, 8.17 g, 72.3 mmol). The mixture is stirred at rt for 2 hours. Aqueous KHSO4 (0.5M, 200 mL) is added and the organic solvents are removed in vacuo to produce an aqueous suspension of the product. The precipitate is collected by filtration, dissolved in IN NaOH and washed two times with ether. The aqueous solution is then acidified to pH<2 with concentrated HCl and a precipitate formed. The precipitate is collected by filtration and washed with 0.5M NaHSO4 then water. The solid is dried in vacuo to give 5.7 g (87%) of 5-(4-chlorophenylsulfanyl)thiophene-2-carboxylic acid. MS for C11H7ClO2S2, (ES) m/z: 269 (M−H)−.

後処理

  1. customthe organic solvents are removed in vacuo
  2. customto produce
  3. additionan aqueous suspension of the product
  4. filtrationThe precipitate is collected by filtration
  5. dissolutiondissolved in IN NaOH
  6. washwashed two times with ether
  7. customa precipitate formed
  8. filtrationThe precipitate is collected by filtration
  9. washwashed with 0.5M NaHSO4
  10. customThe solid is dried in vacuo

出典と根拠

ORDレコード
ord-291cb619609d471896591303a306e1b1
出典データセット
uspto-grants-2003_05
特許番号
US06562816B2

反応ノート

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