HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,2-Trichloroethyl chloroformate → N-(beta,beta,beta-trichloroethoxycarbonyl)-3-pyrroline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,2-Trichloroethyl chloroformate | HCID 87063 | — |
| Reactant | 1-Benzyl-2,5-dihydropyrrole | HCID 561506 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(beta,beta,beta-trichloroethoxycarbonyl)-3-pyrroline | HCID 13192204 | — |
Reaction Steps
40.0 g (0.25 mol) of N-benzyl-3-pyrroline are dissolved in 400 ml of benzene. 53.0 g (0.25 mol) of 2,2,2-trichloroethyl chloroformate are introduced into this solution in the course of 30 minutes, at 0° and under a nitrogen atmosphere. The reaction mixture is stirred for a further 1 hour at 0°, then washed at room temperature twice with, in each case, 100 ml of a mixture of water and 2 N hydrochloric acid (3:1) and then twice with water, dried over sodium sulphate and evaporated under a water pump vacuum. The oily residue is distilled under a high vacuum and, after 24 g of benzyl chloride has been separated off, N-(β,β,β-trichloroethoxycarbonyl)-3-pyrroline with a boiling point of 84°-85° C./0.12 mm Hg is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04160837 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-726ffd3177344721ba902f780bc0581c |
| Source note | uspto-grants-1979_07 |