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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375556Generated: October 27, 2026

Ethanol → 1-(Carboxy)-1-(4-methoxybenzylthio)cyclohexane

https://huagongshe.com/reaction/375556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclohexaneHCID 22400213—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(Carboxy)-1-(4-methoxybenzylthio)cyclohexaneHCID 2121690792%

Reaction Conditions

Temperature60 °C

Reaction Steps

Dissolve 1-(carboethoxy)-1-(4-methoxybenzylthio)cyclohexane (1.45 g, 4.7 mmol) in water (2.5 mL) and tetrahydrofuran (10 mL). Treat with 2.5N sodium hydroxide (4 mL, 10 mmol). Heat at 60° C. for 2 hours, add 95% ethanol (10 mL) and lithium hydroxide monohydrate (0.42 g, 10 mmol) Heat to a gentle reflux for 20 hours, cool and evaporate the solvent in vacuo. Partition between water (50 mL) and ether (50 mL). Separate the aqueous phase and acidify to pH 1. Extract with methylene chloride (50 mL), dry (Na2SO4) and evaporate the solvent in vacuo to give 1-(carboxy)-1-(4-methoxybenzylthio)cyclohexane as a white solid (1.21 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05486513
Source datasetuspto-grants-1996_01
ORD IDord-08060253b8454e1db64e9a7901143a1d
Source noteuspto-grants-1996_01