HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282352Generated: November 1, 2026
4-Chlorobenzoyl chloride → HCID 18424299, compound
https://huagongshe.com/reaction/1282352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 18424242 | HCID 18424242 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 18424299 | HCID 18424299 | — |
Reaction Steps
A solution of 8.43 ml. (0.067 mole) of p-chlorobenzoyl chloride and 8.8 g. (0.067 mole) of aluminum chloride in 100 ml. of 1,2-dichloroethane is added to a solution of 13.0 g. (0.067 mole) of 1-benzylpyrrole-2acetonitrile in 50 ml. of 1,2-dichloroethane at 5° C. over a 5 minute period. The reaction mixture is stirred for 15 minutes and then heated quickly to reflux for 3 minutes. The mixture is poured into ice-hydrochloric acid and then filtered. The aqueous layer is separated and washed with chloroform. The combined organic fractions are washed successively with N,N-dimetylaminopropylamine solution, dilute hydrochloric acid and brine and then dried over anhydrous magnesium sulfate. The solvent is evaporated to yield an oily residue from which the desired compound is isolated by column chromatography on neutral alumina with a 50—50 mixture of benzene ether as the eluting solvent. Evaporation of the elute affords 1-benzyl-5-(p-chlorobenzoyl)-pyrrole-2-acetonitrile as a yellow solid which is recrystallized from methanol, m.p. 106-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06455703B2 |
|---|
| Source dataset | uspto-grants-2002_09 |
|---|
| ORD ID | ord-bca14cf5a3104881a108eba2c11f1f57 |
|---|
| Source note | uspto-grants-2002_09 |
|---|