HCID 21961360, compound → HCID 15516564, compound

HRID 1017846Notes

Reaction equation

HRID 1017846 reaction equation
[CH3:1][C:2]1([CH3:25])[CH2:6][C:5]2[C:7]([CH3:24])=[C:8]([N:13]3[C:21](=O)[C:20]4[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=4)[C:14]3=O)[C:9]([CH3:12])=[C:10]([CH3:11])[C:4]=2[O:3]1>C(O)C>[CH3:1][C:2]1([CH3:25])[CH2:6][C:5]2[C:7]([CH3:24])=[C:8]([N:13]3[CH2:14][C:15]4[C:20](=[CH:19][CH:18]=[CH:17][CH:16]=4)[CH2:21]3)[C:9]([CH3:12])=[C:10]([CH3:11])[C:4]=2[O:3]1

Participants

3

Reactant 1

HCID 21961360HCID 21961360, compound

Product 1

HCID 15516564HCID 15516564, compoundYield 84%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

By using 2-[2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-5-yl]-1H-isoindole-1,3(2H)-dione, the title compound was synthesized according to Example 2a. Yield: 84%. Melting point: 161-163° C. (Ethanol)

Sources & evidence

ORD record
ord-731ed594788649d29d5a89ae10c9b87d
Source dataset
uspto-grants-2002_11
Patent number
US06479536B1

Reaction notes

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