Thionyl Chloride → 4H,5H,6H-cyclopenta[b]thiophen-4-one

HRID 460362

Reaction equation

HRID 460362 reaction equation
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][CH2:7][C:8]([OH:10])=O.O=S(Cl)Cl.[Al+3].[Cl-].[Cl-].[Cl-]>ClCCl>[S:1]1[CH:5]=[CH:4][C:3]2[C:8](=[O:10])[CH2:7][CH2:6][C:2]1=2

Participants

5

Procedure

To a solution of 3-thiophene-2-yl-propionic acid (Intermediate AC) (1.75 g, 0.01122 mol) in dichloromethane (50 mL) was added SOCl2 (1.67 mL, 0.02244 mol) and stirred at room temperature for 6 h. This solution was added dropwise to a suspension of AlCl3 (2.98 g, 0.02244 mol) in dichloromethane (50 mL) over 45 minutes. The resulting mixture was stirred at room temperature for 12 h. The system was quenched by dropwise addition of water (10 mL) and extracted with dichloromethane. The organics were dried with MgSO4 and the solvent was removed in vacuo. The title compound was purified by silica gel column chromatography using 4:1 Hexanes:ethyl acetate as the eluent. MS m/z 139.1 (M+H)+;

Workup

  1. stirringThe resulting mixture was stirred at room temperature for 12 h
  2. customThe system was quenched by dropwise addition of water (10 mL)
  3. extractionextracted with dichloromethane
  4. dry with materialThe organics were dried with MgSO4
  5. customthe solvent was removed in vacuo
  6. customThe title compound was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-c29791c1d5864c2693639fe72ad7a41e
Source dataset
uspto-grants-2007_03
Patent number
US07196110B2

Linked notes

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