HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Methyl 5-(4-chlorophenylthio)pyrrole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Chlorobenzenesulfenylchloride | HCID 11084465 | — |
| Reactant | methyl 1H-pyrrole-3-carboxylate | HCID 12361759 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 5-(4-chlorophenylthio)pyrrole-3-carboxylate | HCID 12897034 | 26.1% |
Reaction Steps
Methyl pyrrole-3-carboxylate (2.5 g., 20 mmole) was dissolved in 35 ml. of methylene chloride. p-Chlorobenzenesulfenyl chloride (4.0 g., 22 mmoles) was added dropwise over approximately 2 minutes, and the reaction mixture was stirred at room temperature for 1 hour. Two volumes of ether were added, the mixture extracted twice with 20 ml. portions of water and the organic layer evaporated in vacuo. The resulting oil was chromatographed on 100 g. of silica gel with approximately 25 ml. fractions of the ethyl acetate-1/hexane-7 eluant collected. Fractions 19 to 36 were combined and concentrated to yield methyl 5-(4-chlorophenylthio)pyrrole-3-carboxylate (1.4 g., m.p. 122°-124° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04511575 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-6467322405d74415b31287602ff7f8ea |
| Source note | uspto-grants-1985_04 |