2-Methyl-7-(trifluoromethyl)quinoline → HCID 178422399, 화합물

HRID 1490913

반응식

HRID 1490913 반응식
Cc1ccc2ccc(C(F)(F)F)cc2n1>C1=CCCC=CCC1.C1=CCCC=CCC1.CC(C)(C)c1ccnc(-c2cc(C(C)(C)C)ccn2)c1.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.COC(C)(C)C.C[OH2+].C[OH2+].[Ir].[Ir]>Cc1cc(B2OC(C)(C)C(C)(C)O2)c2ccc(C(F)(F)F)cc2n1.Cc1ccc2c(B3OC(C)(C)C(C)(C)O3)cc(C(F)(F)F)cc2n1

참가 물질

7

반응물 1

HCID 224169042-Methyl-7-(trifluoromethyl)quinoline

생성물 2

HCID 178422399HCID 178422399, 화합물수율 57%HCID 178422497HCID 178422497, 화합물수율 38%

시약·촉매·용매 4

HCID 2733548Bis(pinacolato)diborane시약HCID 42491874,4'-Di-tert-butyl-2,2'-bipyridyl시약HCID 76001521Bis(1,5-cyclooctadiene)dimethoxydiiridium촉매HCID 15413tert-Butyl methyl ether용매

반응 조건

온도
100 °C

실험 절차

Application of general procedure A to 2-methyl-7-(trifluoromethyl)quinoline (211 mg, 1.00mmol) afforded 2 monoborylated products as a 60:40 ratio.

출처 및 근거

ORD 기록
ord-297c3aeb46f14a219f8a39f08fe03a57
출처 데이터셋
Borylation dataset from Roche

연결된 노트

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