Phosphorus oxychloride → HCID 12851852, compound
Reaction equation
[CH:1]1([C:7]2[C:16]3[C:11](=[C:12]([CH2:17]O)[CH:13]=[CH:14][CH:15]=3)[CH:10]=[CH:9][N:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.P(Cl)(Cl)([Cl:21])=O>>[CH:1]1([C:7]2[C:16]3[C:11](=[C:12]([CH2:17][Cl:21])[CH:13]=[CH:14][CH:15]=3)[CH:10]=[CH:9][N:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
3
Procedure
1-Cyclohexyl-5-hydroxymethylisoquinoline and phosphorus oxychloride were reacted in the same way as in step (g) of Example 13 to afford 1-cyclohexyl-5-chloromethylisoquinoline having a melting point of 88.4° to 89.4° C.
Sources & evidence
- ORD record
- ord-dc0e69c0af604d11bd81513b2f8cbf06
- Source dataset
- uspto-grants-1982_06
- Patent number
- US04337256
Reaction notes
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