2,5-Dichlorobenzyl bromide → HCID 67302930, compound

HRID 888842Notes

Reaction equation

HRID 888842 reaction equation
[CH:1]1([N:8]2[C:11](=[O:12])[C:10]([CH3:14])([CH3:13])[NH:9]2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:15][C:16]1[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][C:17]=1[CH2:18]Br>>[CH:1]1([N:8]2[C:11](=[O:12])[C:10]([CH3:14])([CH3:13])[N:9]2[CH2:18][C:17]2[CH:20]=[C:21]([Cl:24])[CH:22]=[CH:23][C:16]=2[Cl:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1

Participants

3

Reactant 2

HCID 34957442,5-Dichlorobenzyl bromideHCID 67303075HCID 67303075, compound

Product 1

HCID 67302930HCID 67302930, compound

Procedure

2-Cycloheptyl-4,4-dimethyl-1,2-diazetidin-3-one and 2,5-dichlorobenzyl bromide were used for a similar reaction and treatment as Process 6 of Example 1, and the title compound was obtained as a colorless oil.

Sources & evidence

ORD record
ord-4b7d139d33e24739beb587e0cb6126c5
Source dataset
uspto-grants-2012_08
Patent number
US08252781B2

Reaction notes

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