Potassium Hydroxide → 4H,5H,6H-cyclopenta[c]thiophene-5-carboxylic acid

HRID 260700Notes

Reaction equation

HRID 260700 reaction equation
[C:1]([CH:6]1[CH2:13][C:9]2=[CH:10][S:11][CH:12]=[C:8]2[CH2:7]1)([O:3]CC)=[O:2].[OH-].[K+]>C(O)C.O>[C:1]([CH:6]1[CH2:13][C:9]2=[CH:10][S:11][CH:12]=[C:8]2[CH2:7]1)([OH:3])=[O:2]

Participants

5

Reactant 2

HCID 14797Potassium HydroxideHCID 158144125-(Carboethoxy)-2,4,5,6-tetrahydrocyclopenta[c]thiophene

Product 1

HCID 158144134H,5H,6H-cyclopenta[c]thiophene-5-carboxylic acid

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 962WaterSolvent

Procedure

Dissolve 5-(carboethoxy)-2,4,5,6-tetrahydrocyclopenta[c]thiophene (6.68 g, 34.1 mmol) in ethanol (95%, 150 mL) and water (75 mL). Add potassium hydroxide (9.5 g, 0.17mol) and stir at room temperature for 1 hour. Partition between water (150 mL) and ethyl ether (2×150 mL). Acidify the aqueous phase with hydrochloric acid to pH 1. Extract with methylene chloride (2×150 mL), dry (Na2SO4) and evaporate the solvent in vacuo to give 5-(carboxy)-2,4,5,6-tetrahydrocyclopenta [c]thiophene.

Workup

  1. customPartition between water (150 mL) and ethyl ether (2×150 mL)
  2. extractionExtract with methylene chloride (2×150 mL)
  3. dry with materialdry (Na2SO4)
  4. customevaporate the solvent in vacuo

Sources & evidence

ORD record
ord-ce5ff01320c24c62b0db101bd83e08c4
Source dataset
uspto-grants-1996_06
Patent number
US05529996

Reaction notes

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