(Chloromethyl)cyclohexane → HCID 178420897, compound
Reaction equation
[CH:1]1([CH2:7]Cl)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)[N:16]2[CH:20]=[C:19]([CH2:21][O-:22])[N:18]=[CH:17]2)C=CC=CC=1.[Na+]>>[NH:16]1[CH:20]=[C:19]([CH2:21][O:22][CH2:7][CH:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)[N:18]=[CH:17]1Participants
3
Procedure
The preparation is carried out as in Example 36 with cyclohexylmethyl chloride and sodium [1-(triphenylmethyl)imidazol-4-yl]methoxide. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether.
Workup
- customThe title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether
Sources & evidence
- ORD record
- ord-adca1c80bf37432094417255893383ad
- Source dataset
- uspto-grants-1998_01
- Patent number
- US05708171
Reaction notes
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