HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chlorobenzenesulfenyl chloride → Methyl 5-(3-Chlorophenylthio)pyrrole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chlorobenzenesulfenyl chloride | HCID 10154307 | — |
| Reactant | methyl 1H-pyrrole-3-carboxylate | HCID 12361759 | — |
| Product | Methyl 5-(3-Chlorophenylthio)pyrrole-3-carboxylate | HCID 12897032 | — |
Reaction Steps
By the procedure of Example 14, methyl pyrrole-3-carboxylate (2.5 g., 20 mmoles) was reacted with m-chlorobenzenesulfenyl chloride to yield crude product as an oil (5.0 g.). The crude was chromatographed on 250 g. of silica gel, with 100 ml. fractions of the methylene chloride eluant collected. Fractions 17 to 30 were combined and evaporated to yield purified methyl 5-(3-chlorophenylthio)pyrrole-3-carboxylate (1.8 g., m.p. 90°-95° C., m/e 267) which crystallized on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04511575 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-1c9f1b42061c459e9b89ff59cc9eb07f |
| Source note | uspto-grants-1985_04 |