Phenylboronic Acid → HCID 69450238, compound

HRID 1353982Notes

Reaction equation

HRID 1353982 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6](Br)=[C:5]([O:10][CH3:11])[C:4]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH3:18].[C:19]1(B(O)O)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[C:5]([O:10][CH3:11])[C:4]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH3:18]

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 155090951,3-Dimethoxy-2-(Tol-2-yl)-4-Bromobenzene

Product 1

HCID 69450238HCID 69450238, compound

Procedure

This compound was prepared by the same procedure as used in EXAMPLE 3 using 1,3-dimethoxy-2-(tol-2-yl)-4-bromobenzene 2 and phenyl boronic acid to yield 34.

Workup

  1. customThis compound was prepared by the same procedure

Sources & evidence

ORD record
ord-067e0b7161194ee1b1de9b6f8171c875
Source dataset
uspto-grants-2007_05
Patent number
USRE039663E1

Reaction notes

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