Formic Acid → HCID 374038, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([NH2:7])=[O:6].[CH:11](O)=[O:12]>>[CH:11]([NH:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([NH2:7])=[O:6])=[O:12]Participants
3
Procedure
10 gm of 3-aminobenzamide and 80 ml of 98 to 100% formic acid were refluxed for 60 minutes. The formic acid was removed by evaporation under vacuum; the residual oily product was mixed with water and evaporated to yield a solid residue. This solid was crystallized from water to give 8.2 gm (yield=68%) of white, round crystals with a melting point of 176° C. to 177° C. Mass spectrum analysis indicated a molecular weight of 164.
Workup
- customThe formic acid was removed by evaporation under vacuum
- additionthe residual oily product was mixed with water
- customevaporated
- customto yield a solid residue
- customThis solid was crystallized from water
- customto give 8.2 gm (yield=68%) of white, round crystals with a melting point of 176° C. to 177° C
Sources & evidence
- ORD record
- ord-1be7489bc63247839213277e30cc0383
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05719151
Reaction notes
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