Isobutyryl chloride → 5-Isobutyryloxindole

HRID 855741Notes

Reaction equation

[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].[C:11](Cl)(=[O:15])[CH:12]([CH3:14])[CH3:13]>>[C:11]([C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[NH:1][C:2](=[O:10])[CH2:3]2)(=[O:15])[CH:12]([CH3:14])[CH3:13]

Participants

Reactant 2

HCID 62325Isobutyryl chloride

HCID 321710Oxindole

Product 1

HCID 210846465-Isobutyryloxindole

Procedure

Prepared from 2-indolinone and isobutyryl chloride

Sources & evidence

ORD record: ord-768a91ca28504a6aaee3699f71e7d464
Source dataset: uspto-grants-2007_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07262206B2

Reaction notes

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