4-Chlorophenylboronic acid → 4-(4-Chloro-phenyl)-indene
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5](B(O)O)=[CH:4][CH:3]=1.C[Si](C)(C)C1C=CC([C:19]2[CH:27]=[CH:26][CH:25]=[C:24]3[C:20]=2[CH:21]=[CH:22][CH2:23]3)=CC=1>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:19]2[CH:27]=[CH:26][CH:25]=[C:24]3[C:20]=2[CH:21]=[CH:22][CH2:23]3)=[CH:4][CH:3]=1Participants
3
Procedure
The synthesis was performed by the same procedure as in Metallocene Compound A (1-1) by using 4-chlorophenylboronic acid in place of 4-trimethylsilylphenylboronic acid in the synthesis of 4-(4-trimethylsilyl-phenyl)-indene to obtain a white solid of 4-(4-chloro-phenyl)-indene in a yield of 69%.
Sources & evidence
- ORD record
- ord-a2de92e788f04550b034c961893efc53
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09309340B2
Reaction notes
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