2-Phenylindole → HCID 54180223, compound

HRID 355165Notes

Reaction equation

HRID 355165 reaction equation
[C:1]1([C:7]2[NH:8][C:9]3[C:14]([CH:15]=2)=[CH:13][CH:12]=[CH:11][CH:10]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:16][C:17]1=[C:18]([Cl:24])[C:19]([O:21][C:22]1=[O:23])=[O:20]>C(Cl)CCl>[C:1]1([C:7]2[NH:8][C:9]3[C:14]([C:15]=2[C:19](=[O:20])[C:18]([Cl:24])=[C:17]([Cl:16])[C:22]([OH:23])=[O:21])=[CH:13][CH:12]=[CH:11][CH:10]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

4

Reactant 2

HCID 136982-PhenylindoleHCID 70728Dichloromaleic anhydride

Product 1

HCID 54180223HCID 54180223, compound

Reagents, catalysts & solvents 1

HCID 111,2-DichloroethaneSolvent

Procedure

A mixture of 10.0 g (0.052 mole) of 2-phenylindole, 8.8 g (0.052 mole) of dichloromaleic anhydride and 150 ml of ethylene dichloride was stirred at ambient temperature for approximately 48 hours. The solid that formed was collected by filtration and dried at 60° C. in vacuo to obtain 4-(2-phenyl-3-indolyl)-2,3-dichloro-4-oxo-2-butenoic acid (Formula VIII: R=Y=H; R1 =C6H5) as a tan-colored solid which melted over the range 150°-152° C.

Workup

  1. customThe solid that formed
  2. filtrationwas collected by filtration
  3. customdried at 60° C. in vacuo

Sources & evidence

ORD record
ord-ddeb254a183b4a8b9a4d63b7b36744d6
Source dataset
uspto-grants-1983_03
Patent number
US04377698

Reaction notes

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