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Acetamide, N-[(2-chlorophenyl)methyl]-2,2,2-trifluoro- → HCID 178431063, 화합물

HRID 1490750
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HRID 1490750 반응식
O=C(NCc1ccccc1Cl)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(CNC(=O)C(F)(F)F)c(Cl)c2)OC1(C)C.CC1(C)OB(c2ccc(Cl)c(CNC(=O)C(F)(F)F)c2)OC1(C)C
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참가 물질

7

반응물 1

HCID 19165628Acetamide, N-[(2-chlorophenyl)methyl]-2,2,2-trifluoro-

생성물 2

HCID 178431060HCID 178431060, 화합물수율 22%HCID 178431063HCID 178431063, 화합물수율 45%

시약·촉매·용매 4

HCID 2733548Bis(pinacolato)diborane시약HCID 42491874,4'-Di-tert-butyl-2,2'-bipyridyl시약
HCID 76001521Bis(1,5-cyclooctadiene)dimethoxydiiridium촉매
HCID 8028Tetrahydrofuran용매

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온도
35 °C

실험 절차

Following general procedure F using N‐(2‐chlorobenzyl)‐2,2,2‐trifluoroacetamide (59.4 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 solvents removed. Analysis of crude 1 H NMR using internal standard 1,2‐dimethoxyethane showed 5:33:56 dimeta:meta:para borylation in 93% yield. The crude product was purified by silica gel chromatography (Pet. Ether (40‐60):EtOAc (19:1) to give the title compound (as a 4:33:66 mixture of dimeta:meta:para ratio, as determined by 1 H NMR) as a colourless oil (64 mg, 0.18 mmol, 70%). By subtracting the resonances for the meta isomer, the NMR data of the para isomer can be assigned as follows:

출처 및 근거

ORD 기록
ord-db4ef295499d4c659ff8a8620ed53b33
출처 데이터셋
Borylation dataset from Roche
DOI
10.1002/anie.201708967

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