Chlorodiphenylmethane → HCID 18973484, compound

HRID 2394443Notes

Reaction equation

HRID 2394443 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH:10]=[O:11])=[CH:2]1.[CH:12](Cl)([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[CH:12]([N:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH:10]=[O:11])=[CH:2]1)([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

Participants

3

Reactant 2

HCID 7035ChlorodiphenylmethaneHCID 10256Indole-3-Carboxaldehyde

Product 1

HCID 18973484HCID 18973484, compound

Procedure

The same procedures used in Example 1 were repeated except for using 870 mg of indole-3-carbaldehyde and benzhydryl chloride in place of the benzyl bromide used in Example 1 to give 852 mg of 1-benzhydrylindole-3-carbaldehyde as brown crystals. The yield thereof was found to be 46%.

Sources & evidence

ORD record
ord-fa9ea0683a0a4e82ba9c3e0e3420ef45
Source dataset
uspto-grants-1998_09
Patent number
US05811439

Reaction notes

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