HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-BUTYL CHLORIDE → HCID 12415108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-BUTYL CHLORIDE | HCID 10486 | — |
| Reactant | Pyrrole-2-carbonitrile | HCID 138277 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Catalyst | Gallium monochloride | HCID 186022 | — |
| Product | HCID 12415108 | HCID 12415108 | — |
| Product | HCID 18434424 | HCID 18434424 | — |
Reaction Steps
Friedel-Crafts alkylation reactions have been utilized by prior workers to synthesize 4-substituted-pyrrole-2-carbaldehyde compounds. For example, Anderson et.al. (Can. J. Chem. 56, 654-657 (1978)) reacted pyrrole-2-carbonitrile with t-butyl chloride in the presence of aluminum or gallium chloride catalysts, to obtain either 4-t-butyl-pyrrole-2-carbonitrile, or 5-t-butyl-pyrrole-2-carbonitrile. Each of the two isomers of the t-butyl-pyrrole-2-carbonitriles were then reduced to the corresponding aldehydes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441194B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-060e7ec1395b44b6ac1e47b3c5d5cf63 |
| Source note | uspto-grants-2002_08 |