4-Methylbenzoyl Chloride → HCID 12897060, compound
Reaction equation
[C:1]1([CH3:10])[CH:6]=[CH:5][C:4]([C:7](Cl)=[O:8])=[CH:3][CH:2]=1.[NH:11]1[CH:15]=[CH:14][C:13]([C:16]([O:18][CH3:19])=[O:17])=[CH:12]1>>[CH3:10][C:1]1[CH:6]=[CH:5][C:4]([C:7]([C:15]2[NH:11][CH:12]=[C:13]([C:16]([O:18][CH3:19])=[O:17])[CH:14]=2)=[O:8])=[CH:3][CH:2]=1Participants
3
Procedure
Following the procedure of Example 64, p-toluoyl chloride (3.09 g., 20 mmoles) and methyl pyrrole-3-carboxylate were reacted to form methyl 5-(4-methylbenzoyl)pyrrole-3-carboxylate (2.9 g., m.p. 155°-159° C., m/e 243).
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-668d65c0b8084631b1d9167c98c3cd18
- Source dataset
- uspto-grants-1985_04
- Patent number
- US04511576
Reaction notes
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