Phosgene → HCID 13720696, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][CH:8]=[CH:7]2.[C:12](Cl)([Cl:14])=[O:13]>C(Cl)Cl>[N:10]1[C:11]2[C:6](=[CH:5][CH:4]=[CH:3][C:2]=2[NH:1][C:12]([Cl:14])=[O:13])[CH:7]=[CH:8][CH:9]=1Participants
4
Reagents, catalysts & solvents 1
Procedure
8-Aminoquinoline (2.0 g., Pfaltz & Bauer, A28560) in methylene chloride (10 ml) was added dropwise to a 0° C. solution of 2.2M phosgene in methylene chloride (12 ml). The resulting precipitate was filtered and dried. The dark solid thus obtained is unstable and in practice it was immediately used in the next reaction.
Workup
- filtrationThe resulting precipitate was filtered
- customdried
- customThe dark solid thus obtained
- customwas immediately used in the next reaction
Sources & evidence
- ORD record
- ord-dc6bfa4b738245a2b3ec7f3564126b2c
- Source dataset
- uspto-grants-1985_07
- Patent number
- US04530931
Reaction notes
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