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

HRID 1359635노트

반응식

HRID 1359635 반응식
[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

참가 물질

9

실험 절차

The product of Step 33a (6. Ig, 24 mmol) is dissolved in a mixture of THF, t-BuOH, 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 room temperature 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 1N NaOH and washed two times with ether. The aqueous solution is then acidified to pH<6 with concentrated HCl and a precipitate formed. The precipitate is collected by filtration and washed with 0.5M KHSO4 then water. The solid is dried in vacuo to give the product (5.7 g, 87%). MS for C11H7ClO2S2 (ESI) (M−H)− m/z 269.

후처리

  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 1N NaOH
  6. washwashed two times with ether
  7. customa precipitate formed
  8. filtrationThe precipitate is collected by filtration
  9. washwashed with 0.5M KHSO4
  10. customThe solid is dried in vacuo

출처 및 근거

ORD 기록
ord-fe6c173f6baf47e693ae2ddf0fdb0c4e
출처 데이터셋
uspto-grants-2003_07
특허 번호
US06599916B2

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