HCID 155019327, compound → HCID 178503287, compound

HRID 1491166Notes

Reaction equation

HRID 1491166 reaction equation
CSc1cccc(N2CCCC2)c1>C1=CCCC=CCC1.C1=CCCC=CCC1.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.C[OH2+].C[OH2+].Cc1ccc(C)cc1.FC(F)(F)C1COB(c2ccccc2-c2ccc(-c3ccccn3)nc2)O1.[Ir].[Ir]>CSc1cc(N2CCCC2)ccc1B1OC(C)(C)C(C)(C)O1

Participants

6

Reactant 1

HCID 155019327HCID 155019327, compound

Product 1

HCID 178503287HCID 178503287, compoundYield 70%

Reagents, catalysts & solvents 4

HCID 2733548Bis(pinacolato)diboraneReagentHCID 1349566232-Pyridin-2-yl-5-[2-[4-(trifluoromethyl)-1,3,2-dioxaborolan-2-yl]phenyl]pyridineReagentHCID 76001521Bis(1,5-cyclooctadiene)dimethoxydiiridiumCatalystHCID 7809P-XyleneSolvent

Conditions

Temperature
55 °C

Procedure

Ligand 3f: A mixture of ortho- and meta-borylated products (112 mg, 70% yield, ortho/meta + para = >30); ortho-borylated product 4t was obtained by further purification by GPC (99 mg, 62% yield), yellow oil;

Sources & evidence

ORD record
ord-7144e5080f4f4bccabcc2f4319621e6e
Source dataset
Borylation dataset from Roche

Reaction notes

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