2-Acetylphenylboronic acid → 5-(2-Acetylphenyl)-3,3-dimethylindan-1-one

HRID 2251687Notes

Reaction equation

HRID 2251687 reaction equation
[CH3:1][C:2]1([CH3:20])[C:10]2[C:5](=[CH:6][CH:7]=[C:8](OS(C(F)(F)F)(=O)=O)[CH:9]=2)[C:4](=[O:19])[CH2:3]1.[C:21]([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=1B(O)O)(=[O:23])[CH3:22]>>[C:21]([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=1[C:8]1[CH:9]=[C:10]2[C:5](=[CH:6][CH:7]=1)[C:4](=[O:19])[CH2:3][C:2]2([CH3:20])[CH3:1])(=[O:23])[CH3:22]

Participants

3

Reactant 2

HCID 27343092-Acetylphenylboronic acidHCID 57618520Trifluoromethanesulfonic acid 3,3-dimethyl-1-oxo-indan-5-yl ester

Product 1

HCID 690358905-(2-Acetylphenyl)-3,3-dimethylindan-1-one

Procedure

The title compound was prepared from trifluoro-methanesulfonic acid 3,3-dimethyl-1-oxo-indan-5-yl ester and 2-acetylphenyl boronic acid according to the procedure described in example 21. MS (ESI) m/z 279; HRMS: calcd for C19H18O2+H+, 279.13796; found (ESI, [M+H]+), 279.1383.

Sources & evidence

ORD record
ord-1126abde05a344ecbc4b33aeffa8b17b
Source dataset
uspto-grants-2008_01
Patent number
US07319152B2

Reaction notes

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