2-Ethoxycarbonylphenylboronic acid → HCID 23082909, compound

HRID 2422292Notes

Reaction equation

HRID 2422292 reaction equation
Br[C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][CH:21]=1)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][C:15]([O:17]C)=[O:16])=[CH:9][CH:8]=1.[CH2:22]([O:24][C:25]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1B(O)O)=[O:26])[CH3:23]>>[CH2:22]([O:24][C:25]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[C:2]1[CH:21]=[CH:20][CH:19]=[C:4]([CH2:5][O:6][C:7]2[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][C:15]([OH:17])=[O:16])=[CH:9][CH:8]=2)[CH:3]=1)=[O:26])[CH3:23]

Participants

3

Reactant 2

HCID 27734052-Ethoxycarbonylphenylboronic acidHCID 23136270Methyl 4-[(3-bromophenyl)methoxy]benzenepropanoate

Product 1

HCID 23082909HCID 23082909, compound

Procedure

The title compound was synthesized in the same manner as in Example 272 from methyl 3-[4-[(3-bromobenzyl)oxy]phenyl]propanoate and 2-ethoxycarbonylphenylboronic acid. colorless oil (yield 12%).

Sources & evidence

ORD record
ord-73f71e403e81492d83dead3883218160
Source dataset
uspto-grants-2011_06
Patent number
US07960369B2

Reaction notes

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