Phenylboronic Acid → HCID 69037095, compound

HRID 2251676Notes

Reaction equation

HRID 2251676 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]1(B(O)O)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[CH3:1][C:2]1([CH3:20])[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH:9]=2)[C:4](=[O:19])[CH2:3]1

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 57618520Trifluoromethanesulfonic acid 3,3-dimethyl-1-oxo-indan-5-yl ester

Product 1

HCID 69037095HCID 69037095, compound

Procedure

The title compound was prepared from trifluoro-methanesulfonic acid 3,3-dimethyl-1-oxo-indan-5-yl ester and phenyl boronic acid according to the procedure described in example 21. MS m/z 237; HRMS: calcd for C17H16O+H+, 237.12739; found (ESI, [M+H]+), 237.1271.

Sources & evidence

ORD record
ord-e8a1bf3e7e46405fbf465f3d3478c0e4
Source dataset
uspto-grants-2008_01
Patent number
US07319152B2

Reaction notes

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