HCID 101803207, compound → HCID 178431037, compound
Reaction equation
O=C(NCCCc1ccccc1Br)C(F)(F)F>C1=CCCC=CCC1.C1=CCCC=CCC1.C1CCOC1.CC(C)(C)c1ccnc(-c2cc(C(C)(C)C)ccn2)c1.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.C[OH2+].C[OH2+].[Ir].[Ir]>CC1(C)OB(c2ccc(Br)c(CCCNC(=O)C(F)(F)F)c2)OC1(C)C.CC1(C)OB(c2ccc(CCCNC(=O)C(F)(F)F)c(Br)c2)OC1(C)CParticipants
Reactant 1
Product 2
Reagents, catalysts & solvents 4
Conditions
- Temperature
- 35 °C
Procedure
Following general procedure F using N‐(3‐(2‐bromophenyl)propyl)‐2,2,2‐trifluoroacetamide (77.5 mg, 0.25 mmol), B2pin2 (127 mg, 0.50 mmol), [Ir(COD)OMe]2 (2.5 mg, 0.00375 mmol) and dtbpy (2.0 mg, 0.0075 mmol) in THF (1.25 mL). The reaction was stirred at 35 °C for 20 hours before cooling and the solventsremoved. Analysis of crude 1 H NMR using internalstandard 1,2‐dimethoxyethane showed 1:2 meta:para borylation in 93% yield. The crude product was purified by silica gel chromatography (Pet. Ether (40‐60):EtOAc (19:1‐8:1) to give the title compound (as a 1:1.7 mixture of meta:para ratio, as determined by 1 H NMR) as a colourless oil (85.9 mg, 0.20 mmol, 79%). By subtracting the resonances for the meta isomer, the NMR data of the para isomer can be assigned as follows:
Sources & evidence
- ORD record
- ord-19f866d68d3c441a8c9b882b506a5411
- Source dataset
- Borylation dataset from Roche
Reaction notes
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