HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971685Generated: October 29, 2026
m-Chloroperbenzoic acid → HCID 20548869, compound
https://huagongshe.com/reaction/971685
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 20548897 | HCID 20548897 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20548869 | HCID 20548869 | — |
Reaction Steps
100 g (0.38 mol) of 1-(β,β,β-trichloroethoxycarbonyl)-1,2,5,6-tetrahydropyridine are dissolved in 1,200 ml of methylene chloride and the solution is treated with 157 g (0.77 mol) of 85% strength m-chloroperbenzoic acid in portions. The slightly exothermic reaction is kept at room temperature by means of a water bath. After the addition has ended (which takes about 2 hours), the reaction mixture, in which a white suspension forms, is stirred for a further 15 hours at room temperature. The m-chlorobenzoic acid which has precipitated is filtered off and the filtrate is washed with a saturated aqueous solution of sodium carbonate, then with aqueous iron-II sulphate solution, then with 0.1 N sodium hydroxide solution and finally with water, dried over sodium sulphate and evaporated under a water pump vacuum. The oil which remains is dissolved in 100 ml of benzene and the solution is filtered through a layer of silica gel. Elution with a benzene/ethyl acetate mixture (1:1) and evaporation of the solvent gives pure 3,4-epoxy-1-(β,β,β-trichloroethoxycarbonyl)-piperidine in the form of a slightly orange coloured oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04160837 |
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| Source dataset | uspto-grants-1979_07 |
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| ORD ID | ord-bbda8cc1e2b24ac7be2c49d6fc265d79 |
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| Source note | uspto-grants-1979_07 |
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