Naphthalen-2-yl(phenyl)methanol → 3-Hydroxy-4-methyl-2-(naphthalen-2-yl-phenyl-methyl)-4-phenyl-cyclobut-2-enone

HRID 646079

Reaction equation

HRID 646079 reaction equation
[CH3:1][C:2]1([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:5](=[O:6])[CH2:4][C:3]1=[O:7].[CH:14]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=[CH:16][C:15]=1[CH:24]([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)O>>[OH:6][C:5]1[C:2]([CH3:1])([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:3](=[O:7])[C:4]=1[CH:24]([C:15]1[CH:16]=[CH:17][C:18]2[C:23](=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:14]=1)[C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1

Participants

3

Procedure

Using general procedure D, 2-methyl-2-phenyl-cyclobutane-1,3-dione (Lit. 1) was reacted with naphthalen-2-yl-phenyl-methanol to give the title compound as a colorless solid. MS: 389.5 ([M−H]−).

Sources & evidence

ORD record
ord-8aec4578406749d29874692f4c118e61
Source dataset
uspto-grants-2010_04
Patent number
US07705034B2

Linked notes

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