Ethyl 2-oxocyclohexylacetate → HCID 17913392, compound

HRID 2165572Notes

Reaction equation

HRID 2165572 reaction equation
Cl.[Cl:2][C:3]1[CH:17]=[CH:16][C:6]([CH2:7][N:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)N)=[CH:5][CH:4]=1.[CH3:18][CH2:19][O:20][C:21]([CH2:23][CH:24]1[C:29](=O)[CH2:28][CH2:27][CH2:26][CH2:25]1)=[O:22]>>[Cl:2][C:3]1[CH:17]=[CH:16][C:6]([CH2:7][N:8]2[C:25]3[CH:24]([CH2:23][C:21]([O:20][CH2:19][CH3:18])=[O:22])[CH2:29][CH2:28][CH2:27][C:26]=3[C:15]3[C:10]2=[CH:11][CH:12]=[CH:13][CH:14]=3)=[CH:5][CH:4]=1

Participants

3

Reactant 2

HCID 91229Ethyl 2-oxocyclohexylacetateHCID 14591231HCID 14591231, compound

Product 1

HCID 17913392HCID 17913392, compound

Procedure

Following the procedure of Example 1, but using 1-(4-chlorobenzyl)-1-(phenyl)hydrazine hydrochloride and ethyl 2-cyclohexanone acetate as starting materials, the title compound was prepared.

Sources & evidence

ORD record
ord-c5dc7466009840e79fedd1abd664db20
Source dataset
uspto-grants-1990_07
Patent number
US04940719

Reaction notes

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