1-Bromononane → 1-Nonyl-7-phenyl-indoline-2,3-dione

HRID 1071566Notes

Reaction equation

Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[C:11]1([C:17]2[CH:18]=[CH:19][CH:20]=[C:21]3[C:25]=2[NH:24][C:23](=[O:26])[C:22]3=[O:27])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[CH2:2]([N:24]1[C:25]2[C:21](=[CH:20][CH:19]=[CH:18][C:17]=2[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:22](=[O:27])[C:23]1=[O:26])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]

Participants

Reactant 2

HCID 127421-Bromononane

HCID 107754477-Phenylisatin

Product 1

HCID 5084221-Nonyl-7-phenyl-indoline-2,3-dione

Procedure

The title compound was prepared in a manner similar to the process step described in the text from Page 7, line 34 to Page 8, line 5 of WO 94/29272 but using a haloalkane such as 1-bromononane together with 7-phenyl-1H-indole-2,3-dione.

Sources & evidence

ORD record: ord-4cac5af8af454fae842e64f8cd411a3f
Source dataset: uspto-grants-2005_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06906090B1

Reaction notes

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