2-Cyclohexylethanol → 4-[4-Benzyloxy-2-(2-cyclohexylethoxy)-3-ethylphenoxy]-5-methyl-7-nitroindane

HRID 1766683Notes

Reaction equation

HRID 1766683 reaction equation
[CH2:1]([O:8][C:9]1[C:10]([CH2:30][CH3:31])=[C:11]([OH:29])[C:12]([O:15][C:16]2[C:24]([CH3:25])=[CH:23][C:22]([N+:26]([O-:28])=[O:27])=[C:21]3[C:17]=2[CH2:18][CH2:19][CH2:20]3)=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:32]1([CH2:38][CH2:39]O)[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]1>>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][C:16]2[C:24]([CH3:25])=[CH:23][C:22]([N+:26]([O-:28])=[O:27])=[C:21]3[C:17]=2[CH2:18][CH2:19][CH2:20]3)=[C:11]([O:29][CH2:39][CH2:38][CH:32]2[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]2)[C:10]=1[CH2:30][CH3:31])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 205082-CyclohexylethanolHCID 230311123-Benzyloxy-2-ethyl-6-(5-methyl-7-nitroindan-4-yloxy)phenol

Product 1

HCID 211105774-[4-Benzyloxy-2-(2-cyclohexylethoxy)-3-ethylphenoxy]-5-methyl-7-nitroindane

Procedure

The title compound was prepared in a similar manner to those described in Example 2 using 3-benzyloxy-2-ethyl-6-(5-methyl-7-nitroindan-4-yloxy)phenol instead of ethyl N-[7-(3-ethyl-2-hydroxy-4-trifluoromethanesulfonyloxyphenoxy)-6-methylindan-4-yl]malonamate and using 2-cyclohexylethanol instead of 4-fluorobenzylalcohol.

Sources & evidence

ORD record
ord-971fb69be90344ab968401347ea36001
Source dataset
uspto-grants-2007_06
Patent number
US07230031B2

Reaction notes

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