Formic Acid → N-Pyridin-2-ylmethyl-formamide
Reaction equation
[NH2:1][CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][N:4]=1.[CH:9](O)=[O:10]>>[CH:9]([NH:1][CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][N:4]=1)=[O:10]Participants
3
Procedure
2-Aminomethylpyridine (60 g.) was refluxed with 180 ml. of formic acid for 4 hours and left to stir for approximately 16 hours at room temperature. The reaction mixture was concentrated to an oil and purified; 2-formamidomethylpyridine obtained by distillation (72.3 g., b.p. 117°-141° C./0.5 mm.)
Workup
- waitleft
- concentrationThe reaction mixture was concentrated to an oil
- custompurified
Sources & evidence
- ORD record
- ord-ab1b352a26db4370a11f54d3e7d9d065
- Source dataset
- uspto-grants-1985_04
- Patent number
- US04511576
Reaction notes
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