HCID 23113870, compound → HCID 23114085, compound

HRID 1787158Notes

Reaction equation

HRID 1787158 reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:14]3[C:15]([CH3:21])=[C:16]([CH3:20])[C:17]([CH3:19])=[CH:18][C:13]=3[O:12][CH:11]=2)=[CH:6][CH:5]=1)([CH3:3])[CH3:2]>CO>[CH:1]([C:4]1[CH:5]=[CH:6][C:7]([CH:10]2[C:14]3[C:15]([CH3:21])=[C:16]([CH3:20])[C:17]([CH3:19])=[CH:18][C:13]=3[O:12][CH2:11]2)=[CH:8][CH:9]=1)([CH3:3])[CH3:2]

Participants

3

Reactant 1

HCID 23113870HCID 23113870, compound

Product 1

HCID 23114085HCID 23114085, compoundYield 74%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Using 3-(4-isopropylphenyl)-4,5,6-trimethyl-1-benzofuran obtained in Reference Example 194, the title compound was synthesized in the same manner as in Reference Example 199. Yield 74%. Melting point: 70-71° C. (methanol).

Workup

  1. customobtained in Reference Example 194

Sources & evidence

ORD record
ord-1507f54fa3714afcbb767b79755eb5f1
Source dataset
uspto-grants-2009_03
Patent number
US07507841B2

Reaction notes

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