HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585325Generated: November 1, 2026
Thionyl Chloride → Ethyl 4-(chlorocarbonyl)-1-piperidinecarboxylate
https://huagongshe.com/reaction/1585325
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(Ethoxycarbonyl)-4-piperidinecarboxylic Acid | HCID 6618886 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 4-(chlorocarbonyl)-1-piperidinecarboxylate | HCID 11096122 | — |
Reaction Steps
A solution of 578.2 g of 4-carboxy-1-ethoxycarbonylpiperidine in 1200 ml of toluene is treated firstly with 1.0 g of N,N-dimethylformnamide and then, at from 68 to 70° C. and within the space of 2 hours, with 369.0 g of thionyl chloride. The mixture is subsequently stirred at 70° C. for a further 30 min, after which the toluene is distilled off in vacuo and the residue is then degassed at RT for approximately 30 min under HV. This results in the title compound in the form of a weakly yellow oil [IR (Film): 2960, 2870, 1790, 1695, 1470, 1435, 1300, 1230, 1130, 960, 765 cm-1 ]. The product distils without decomposition at a m.p. of 96-98° C. (0.08-0.09 Torr).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05935976 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-21a3576b5209402aade3fd8b376a7dad |
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| Source note | uspto-grants-1999_08 |
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