2-(4-Chlorophenoxy)-1-phenylethanone → HCID 44220087, compound

HRID 1402917Notes

Reaction equation

HRID 1402917 reaction equation
ClC1C=CC(OCC(C2C=CC=CC=2)=O)=CC=1.[Cl:18][C:19]1[CH:39]=[CH:38][C:22]([O:23][CH2:24]/[C:25](/[C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)=[CH:26]\[C:27]([O:29][CH2:30][CH3:31])=[O:28])=[CH:21][CH:20]=1>>[Cl:18][C:19]1[CH:20]=[CH:21][C:22]([O:23][CH2:24]/[C:25](/[C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)=[CH:26]/[C:27]([O:29][CH2:30][CH3:31])=[O:28])=[CH:38][CH:39]=1

Participants

3

Reactant 2

HCID 3095712-(4-Chlorophenoxy)-1-phenylethanoneHCID 14920033HCID 14920033, compound

Product 1

HCID 44220087HCID 44220087, compound

Procedure

By a procedure similar to that of example 1.85.3, starting from 2-(4-chlorophenoxy)-1-phenylethanone, (Z)-ethyl 4-(4-chlorophenoxy)-3-phenylbut-2-enoate and (E)-ethyl 4-(4-chlorophenoxy)-3-phenylbut-2-enoate were obtained as colourless oils.

Sources & evidence

ORD record
ord-812ec76780e744dbb7834bdf9961a97a
Source dataset
uspto-grants-2014_12
Patent number
US08912186B2

Reaction notes

Loading…