3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride) → HCID 69038344, compound

HRID 2251677Notes

Reaction equation

HRID 2251677 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.[Cl:21][C:22]1[CH:23]=[C:24](B(O)O)[CH:25]=[CH:26][C:27]=1[F:28]>>[Cl:21][C:22]1[CH:23]=[C:24]([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:25]=[CH:26][C:27]=1[F:28]

Participants

3

Procedure

The title compound was prepared from trifluoro-methanesulfonic acid 3,3-dimethyl-1-oxo-indan-5-yl ester and 3-chloro-4-fluorophenyl boronic acid according to the procedure described in example 21. MS m/z 289; HRMS: calcd for C17H14ClFO+H+, 289.07900; found (ESI, [M+H]+), 289.0785.

Sources & evidence

ORD record
ord-67f4e6a9873046279e4844611dad295a
Source dataset
uspto-grants-2008_01
Patent number
US07319152B2

Reaction notes

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