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3-Bromoanisole → 1-(3-Methoxyphenyl)piperidine-4-carbonitrile

HRID 296
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HRID 296 반응식
COc1cccc(Br)c1.N#CC1CCNCC1>CC(=O)O.CC(=O)O.CC(C)CN1CCN2CCN(CC(C)C)P1N(CC(C)C)CC2.C[Si](C)(C)[N-][Si](C)(C)C.Cc1ccccc1.[Li+].[Pd]>COc1cccc(N2CCC(C#N)CC2)c1
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참가 물질

7

반응물 2

HCID 169713-BromoanisoleHCID 1382234-Cyanopiperidine

생성물 1

HCID 1170033531-(3-Methoxyphenyl)piperidine-4-carbonitrile수율 54.48%

시약·촉매·용매 4

HCID 2733832Lithium hexamethyldisilazane시약HCID 4144353Palladium (II) acetate촉매
HCID 4571243
2,8,9-Triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo(3.3.3)undecane
촉매
HCID 1140Toluene용매

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온도
100 °C

실험 절차

piperidine-4-carbonitrile (0.353 g, 3.21 mmol); 1-bromo-3-methoxybenzene (0.339 mL, 2.67 mmol) and diacetoxypalladium (0.120 g, 0.53 mmol) were thoroughly placed under an inert atmoshere. To this was added 2,8,9-triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane (0.037 g, 0.11 mmol); LITHIUM BIS(TRIMETHYLSILYL)AMIDE (6.15 mL, 6.15 mmol) and toluene (10 mL). The resultant mixture was stirred overnight at 100 °C (suspect that it did not need overnight. Equal vol of DCM was added and the reaction mixture filtered. Removal of the solvent under reduced pressure gave a dark brown gum. The crude product was purified by flash Silica chromatography {CombiFlash Companion - Presearch Ltd}, column size = 12 g , flow rate = 30 ml / min, elution gradient 0 to 30% EtOAc in isohexane over 10 minutes {excluding lead in & wash etc.}. Pure fractions were evaporated to dryness to afford 1-(3-methoxyphenyl)piperidine-4-carbonitrile (0.315 g, 54.5 %) as a tan brown solid.

출처 및 근거

ORD 기록
ord-fa6037d0d8a544539857cac2da5223a4
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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