Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | (1H-Pyrrol-2-yl)-acetonitrile | HCID 13067931 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18424273 | HCID 18424273 | — |
Reaction Steps
To a chilled suspension of 26.80 g. (0.2 mole) of aluminum chloride in 110 ml. of methylene chloride is added dropwise 35 g. (0.2 mole) of p-chlorobenzoyl chloride. The mixture is added dropwise to a solution of 21.22 g. (0.2 mole) of pyrrole-2-acetonitrile in 125 ml. methylene chloride which is cooled externally with an ammonium chloride ice bath. After addition is complete, the reaction mixture is stirred for ten minutes at 0°C. and then poured into ice acidified with dilute hydrochloric acid. A solid precipitate, 5-(p-chlorobenzoyl)-pyrrole-2-acetonitrile, which is filtered off, washed with hot methanol and dried, m.p. 203°-205°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03952012 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-811a22043c6441e59c5861e856c6f4cf |
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| Source note | uspto-grants-1976_04 |
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