1-Naphthaleneboronic acid → {10-[4-(Naphthalen-1-yl)phenyl]anthracen-9-yl}boronic acid

HRID 1045285Notes

Reaction equation

HRID 1045285 reaction equation
[C:1]1([B:11]([OH:13])[OH:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[CH:14]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=[CH:16][C:15]=1B(O)O>>[C:14]1([C:1]2[CH:10]=[CH:5][C:4]([C:4]3[C:3]4[C:2](=[CH:6][CH:7]=[CH:8][CH:9]=4)[C:1]([B:11]([OH:13])[OH:12])=[C:10]4[C:5]=3[CH:6]=[CH:7][CH:8]=[CH:9]4)=[CH:3][CH:2]=2)[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=[CH:16][CH:15]=1

Participants

3

Reactant 2

HCID 2545321-Naphthaleneboronic acidHCID 2734375(Naphthalen-2-yl)boronic acid

Product 1

HCID 23148600{10-[4-(Naphthalen-1-yl)phenyl]anthracen-9-yl}boronic acid

Procedure

10-(4-Naphthalene-1-yl-phenyl)anthracene-9-boronic acid was synthesized by the same method, except that in Synthetic Example 1, 1-naphthaleneboronic acid was used as a starting material in place of 2-naphthaleneboronic acid.

Sources & evidence

ORD record
ord-347ec8fcd5f54979bdf5287a0fb02749
Source dataset
uspto-grants-2013_10
Patent number
US08568902B2

Reaction notes

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