HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163666Generated: November 2, 2026
Ethyl Thioglycolate → HCID 12414524, compound
https://huagongshe.com/reaction/2163666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | Methyl 1-benzoyl-4-oxo-3-piperidinecarboxylate | HCID 12414561 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12414524 | HCID 12414524 | — |
Reaction Steps
A solution of 1-benzoyl-3-methoxycarbonyl-4-piperidone (12 g; 0.046 mole) in absolute ethanol (150 cc), cooled to -10° C, is saturated with dry hydrochloric gas. Ethyl mercapto-acetate (10.8 g; 0.092 mole) is added thereto and a slight stream of hydrochloric gas is further passed therethrough at -10° C during 5 hours. After leaving the reaction mixture aside at room temperature during 70 hours, it is evaporated to dryness and the residue is dissolved in ether. The organic phase is washed with a 5% sodium bicarbonate solution and with water, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting 1-benzoyl-4-ethoxycarbonylmethylthio-3-methoxycarbonyl-1,2,5,6-tetrahydro-pyridine is obtained as an oil (Yield: 100%) and used directly in the next step:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04136186 |
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| Source dataset | uspto-grants-1979_01 |
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| ORD ID | ord-7e7c6b2fc3f44e4988795b4c08070923 |
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| Source note | uspto-grants-1979_01 |
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