Ammonium Chloride → HCID 19705215, compound

HRID 727157Notes

Reaction equation

[C:1]1([CH:7]2[CH2:12][CH2:11][C:10](=[O:13])[CH:9]=[CH:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:14][Li].[Cl-].[NH4+]>>[CH3:14][CH:8]1[CH:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH2:12][CH2:11][C:10](=[O:13])[CH2:9]1

Participants

Reactant 3

HCID 25517Ammonium Chloride

HCID 110628762-Cyclohexen-1-one, 4-phenyl-

HCID 178418348HCID 178418348, compound

Product 1

HCID 19705215HCID 19705215, compound

Procedure

The intermediate 3-methyl-4-phenylcyclohexanone is prepared, first by the reaction of 4-phenylcyclohexanone with phenylselenenyl chloride and aqueous 30% hydrogen peroxide, yielding 4-phenyl-2-cyclohexenone, and then the reaction of the cyclohexenone with 1.4M methyllithium and aqueous ammonium chloride, affording 3-methyl-4-phenylcyclohexanone. The cyclohexanone is then reacted with cyanoguanidine as previously described. Example 15 provides a detailed description of how this reaction is conducted.

Sources & evidence

ORD record: ord-aa165bcc715c4716b7ba04b2fdbf3a21
Source dataset: uspto-grants-1998_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05712281

Reaction notes

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