3-Ethylsulfonylphenylboronic acid → HCID 69036860, compound

HRID 2251683Notes

Reaction equation

HRID 2251683 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.[CH2:21]([S:23]([C:26]1[CH:27]=[C:28](B(O)O)[CH:29]=[CH:30][CH:31]=1)(=[O:25])=[O:24])[CH3:22]>>[CH2:21]([S:23]([C:26]1[CH:31]=[C:30]([C:8]2[CH:9]=[C:10]3[C:5](=[CH:6][CH:7]=2)[C:4](=[O:19])[CH2:3][C:2]3([CH3:1])[CH3:20])[CH:29]=[CH:28][CH:27]=1)(=[O:24])=[O:25])[CH3:22]

Participants

3

Reactant 2

HCID 164271023-Ethylsulfonylphenylboronic acidHCID 57618520Trifluoromethanesulfonic acid 3,3-dimethyl-1-oxo-indan-5-yl ester

Product 1

HCID 69036860HCID 69036860, compound

Procedure

The title compound was prepared from trifluoro-methanesulfonic acid 3,3-dimethyl-1-oxo-indan-5-yl ester and 3-(ethylsulfonyl)phenyl boronic acid according to the procedure described in example 21. MS m/z 329; HRMS: calcd for C19H20O3S+H+, 329.12059; found (ESI, [M+H]+), 329.1217.

Sources & evidence

ORD record
ord-5629189c5a3e404ca1e17243e82804a4
Source dataset
uspto-grants-2008_01
Patent number
US07319152B2

Reaction notes

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