Potassium Hydroxide → 1-(Carboxy)-1-(4-methoxybenzylthio)cyclopentane

HRID 1451243Notes

Reaction equation

HRID 1451243 reaction equation
[C:1]([C:5]1([S:10][CH2:11][C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)[CH2:9][CH2:8][CH2:7][CH2:6]1)([O:3]C)=[O:2].[OH-].[K+]>C(O)C.O.O1CCCC1>[C:1]([C:5]1([S:10][CH2:11][C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)[CH2:9][CH2:8][CH2:7][CH2:6]1)([OH:3])=[O:2]

Participants

6

Reactant 2

HCID 14797Potassium HydroxideHCID 158143811-(Carbomethoxy)-1-(4-methoxybenzylthio)cyclopentane

Product 1

HCID 158143821-(Carboxy)-1-(4-methoxybenzylthio)cyclopentaneYield 72%

Reagents, catalysts & solvents 3

HCID 702EthanolSolventHCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Procedure

Dissolve 1-(carbomethoxy)-1-(4-methoxylbenzylthio)cyclopentane (3.3 mmol) in 95% ethanol (18 mL), water (9 mL), and tetrahydrofuran (10 mL). Treat with potassium hydroxide (0.91 g, 16 mmol). Stir at room temperature for 2 hours and evaporate the solvent in vacuo. Partition between water (50 mL) and ethyl ether (30 mL). Acidify the aqueous phase with cold concentrated hydrochloric acid and extract with methylene chloride (50 mL). Dry (MgSO4) and evaporate the solvent in vacuo to give 1-(carboxy)-1-(4-methoxybenzylthio)cyclopentane as a pale yellow oil (483 mg, 72%).

Workup

  1. customevaporate the solvent in vacuo
  2. customPartition between water (50 mL) and ethyl ether (30 mL)
  3. extractionextract with methylene chloride (50 mL)
  4. dry with materialDry (MgSO4)
  5. customevaporate the solvent in vacuo

Sources & evidence

ORD record
ord-f7ea82016567402e9631bf0a8bdcb6fb
Source dataset
uspto-grants-1997_02
Patent number
US05604221

Reaction notes

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