Sulfuric Acid → 5-(Carbomethoxy)-2,4,5,6-tetrahydro-cyclopenta[c]thiophene
Reaction equation
[C:1]([CH:4]1[CH2:11][C:7]2=[CH:8][S:9][CH:10]=[C:6]2[CH2:5]1)([OH:3])=[O:2].[CH3:12]OC(OC)(C)C.S(=O)(=O)(O)O>CO>[C:1]([CH:4]1[CH2:11][C:7]2=[CH:8][S:9][CH:10]=[C:6]2[CH2:5]1)([O:3][CH3:12])=[O:2]Participants
5
Procedure
Dissolve 5-(carboxy)-2,4,5,6-tetrahydrocyclopenta[c]thiophene (3.95 g, 23.5 mmol) in methanol (60 mL) and treat with dimethoxypropane (5.8 mL, 47 mmol) and sulfuric acid (0.8 mL). Stir at room temperature for 1 day. Evaporate the solvent in vacuo, dilute with methylene chloride (75 mL) and wash with saturated sodium hydrogen carbonate (35 mL). Extract the aqueous phase with methylene chloride (30 mL), wash combined organics with brine (30 mL) and dry (Na2SO4). Evaporate the solvent in vacuo and pass through a plug of silica gel to give 5-(carbomethoxy)-2,4,5,6-tetrahydro-cyclopenta[c]thiophene.
Workup
- customEvaporate the solvent in vacuo
- additiondilute with methylene chloride (75 mL)
- washwash with saturated sodium hydrogen carbonate (35 mL)
- extractionExtract the aqueous phase with methylene chloride (30 mL)
- washwash
- dry with materialdry (Na2SO4)
- customEvaporate the solvent in vacuo and pass through a plug of silica gel
Sources & evidence
- ORD record
- ord-08dab0427af14ec18c8c42dfbec30973
- Source dataset
- uspto-grants-1995_06
- Patent number
- US05428158
Reaction notes
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