Methyl Isocyanate → HCID 20074946, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]([CH2:11][C:12]([O:14]C)=O)[NH2:10])=[CH:5][CH:4]=1.[CH3:16][N:17]=[C:18]=[O:19].C[O-].[Na+]>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([N:9]2[CH2:11][C:12](=[O:14])[N:17]([CH3:16])[C:18](=[O:19])[NH:10]2)=[CH:7][CH:8]=1Participants
4
Procedure
Methyl [1-(4-methoxyphenyl)hydrazino]acetate (1.50 g) was treated with methyl isocyanate (0.85 ml) and then with sodium methoxide (from sodium (0.33 g) in methanol (15 ml)) according to the method of Example 1. The product was purified by recrystallisation from ethyl acetate to give the title compound (703 mg), m.p. 179°-181°, t.l.c. (ether) Rf 0.5.
Workup
- customThe product was purified by recrystallisation from ethyl acetate
Sources & evidence
- ORD record
- ord-59beabe91c7046c4aea733ef5fa260f6
- Source dataset
- uspto-grants-1991_01
- Patent number
- US04985427
Reaction notes
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