Trimethyl borate → HCID 22285289, compound

Reaction equation

[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=1.[B:14](OC)([O:17]C)[O:15]C>>[F:1][C:2]1[C:3]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=2)=[CH:4][CH:5]=[CH:6][C:7]=1[B:14]([OH:17])[OH:15]

Participants

Reactant 2

HCID 8470Trimethyl borate

HCID 98555982-(2-Fluorophenyl)pyridine

Product 1

HCID 22285289HCID 22285289, compound

Procedure

2-(2-Fluorophenyl)pyridine was lithiated and reacted with trimethyl borate as described in Example 31 to give 2-fluoro-3-(pyridin-2-yl)benzeneboronic acid as a white solid: m/z (ES+) 218 (M++H).

Sources & evidence

ORD record: ord-6900c716e4024bebb78228968b12f017
Source dataset: uspto-grants-2005_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06900215B2

Reaction notes

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