HCID 23114059, compound → HCID 23114178, compound

HRID 1787154Notes

Reaction equation

HRID 1787154 reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10](=O)[CH2:11][O:12][C:13]2[CH:21]=[C:20]([CH3:22])[CH:19]=[C:18]3[C:14]=2[CH2:15][CH2:16][CH2:17]3)=[CH:6][CH:5]=1)([CH3:3])[CH3:2]>CO>[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:21]3[C:20]([CH3:22])=[CH:19][C:18]4[CH2:17][CH2:16][CH2:15][C:14]=4[C:13]=3[O:12][CH:11]=2)=[CH:6][CH:5]=1)([CH3:3])[CH3:2]

Participants

3

Reactant 1

HCID 23114059HCID 23114059, compound

Product 1

HCID 23114178HCID 23114178, compoundYield 77%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Using 1-(4-isopropylphenyl)-2-((6-methyl-2,3-dihydro-1H-inden-4-yl)oxy)ethanone obtained in Reference Example 180, the title compound was synthesized in the same manner as in Reference Example 143. Yield 77%. Melting point: 70-72° C. (methanol).

Workup

  1. customobtained in Reference Example 180

Sources & evidence

ORD record
ord-7c6e8c103d3b43209cfdc53cab01544f
Source dataset
uspto-grants-2009_03
Patent number
US07507841B2

Reaction notes

Loading…