Phenylboronic Acid → HCID 22557638, compound

HRID 1268323Notes

Reaction equation

HRID 1268323 reaction equation
Br[C:2]1[CH:3]=[C:4](/[CH:9]=[CH:10]/[C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:5]=[C:6](Br)[CH:7]=1.[C:16]1(B(O)O)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[C:16]1([C:2]2[CH:3]=[C:4](/[CH:9]=[CH:10]/[C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:5]=[C:6]([C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[CH:7]=2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 16215805HCID 16215805, compound

Product 1

HCID 22557638HCID 22557638, compound

Procedure

The colourless solid, (E)-ethyl 3-[1,1′;3′,1″]terphenyl-5′-yl-acrylate was prepared from (E)-ethyl 3-(3,5-dibromophenyl)-acrylate and phenylboronic acid by a procedure analogous to that described in example 52a.

Sources & evidence

ORD record
ord-57a3f21592ea43948357916b5aa7b59f
Source dataset
uspto-grants-2003_04
Patent number
US06555577B1

Reaction notes

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