Pyridine → HCID 14552672, compound
Reaction equation
[CH3:1][C:2]([CH3:17])=[CH:3][CH2:4][O:5][C:6]1[CH:16]=[CH:15][C:9]([O:10][CH:11]([CH3:14])[CH2:12][NH2:13])=[CH:8][CH:7]=1.Cl[C:19]([O:21][CH2:22][CH3:23])=[O:20].N1C=CC=CC=1>>[CH3:17][C:2]([CH3:1])=[CH:3][CH2:4][O:5][C:6]1[CH:7]=[CH:8][C:9]([O:10][CH:11]([CH3:14])[CH2:12][NH:13][C:19](=[O:20])[O:21][CH2:22][CH3:23])=[CH:15][CH:16]=1Participants
4
Procedure
Following the procedure of Example 8, the above propylamine (2.0 g, 8.5 mmol) and ethyl chloroformate (1.01 g, 9.35 mmol) are reacted together, in the presence of pyridine (0.74 g, 9.35 mmol), to give ethyl N-{2-[4-(3-methyl-2-butenoxy)phenoxy]propyl}carbamate, MS m/e 307 (M+).
Sources & evidence
- ORD record
- ord-4de18bcda0854263b5829d74a9de2976
- Source dataset
- uspto-grants-1990_11
- Patent number
- US04968829
Reaction notes
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