HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236334Generated: October 25, 2026
2-Chloroethyl formate → 1-Ethoxycarbonyl-4-ethoxycarbonyl-mercapto-piperidine
https://huagongshe.com/reaction/236334
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethyl formate | HCID 246748 | — |
| Reactant | 1-Methyl-4-ethoxycarbonyl-mercapto-piperidine | HCID 19813381 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Ethoxycarbonyl-4-ethoxycarbonyl-mercapto-piperidine | HCID 20216974 | — |
Reaction Steps
106.3 g (0.88 mol) of chloroethylformate are added dropwise with stirring over a period of 30 minutes to a solution of 100 g (0.48 mol) of 1-methyl-4-ethoxycarbonyl-mercapto-piperidine in 80 ml of toluene which has been heated to 90° C. The solution is then heated for two hours to from 100° to 110° C. After repeated addition of 40 g of chloroethylformate the solution is heated for a further three hours. After leaving it to stand overnight at room temperature it is drawn off by suction using a glass fibre filter. The solution is concentrated on a rotary evaporator and the residue is distilled off. 20 g (94% of the theoretical yield) of 1-ethoxycarbonyl-4-ethoxycarbonyl-mercapto-piperidine are obtained. B.P. 138°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04643995 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-1a343854b68b4651b8f9da0712b06283 |
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| Source note | uspto-grants-1987_02 |
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