HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22519Generated: October 27, 2026
Ethanol → 1-(Carboxy)-1-(4-methoxybenzylthio)cyclohexane
https://huagongshe.com/reaction/22519
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | 1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclohexane | HCID 22400213 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Carboxy)-1-(4-methoxybenzylthio)cyclohexane | HCID 21216907 | — |
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 (l.21 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05428158 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-e57f3bdf09de44f283081084229aa7b8 |
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| Source note | uspto-grants-1995_06 |
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