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4-Bromophenol → 4-(4-Methyl-1-piperazinyl)phenol

HRID 243
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인쇄 미리보기

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HRID 243 반응식
CN1CCNCC1.Oc1ccc(Br)cc1>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]>CN1CCN(c2ccc(O)cc2)CC1
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참가 물질

7

반응물 2

HCID 78084-BromophenolHCID 531671-Methylpiperazine

생성물 1

HCID 116224864-(4-Methyl-1-piperazinyl)phenol수율 50.99%

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
80 °C

실험 절차

diacetoxypalladium (0.039 g, 0.17 mmol) was added in one portion to 4-bromophenol (3 g, 17.34 mmol) and 1-methylpiperazine (2.308 mL, 20.81 mmol) in toluene (87 mL) at 25°C under nitrogen. To this was added toluene (87 mL) then a solution of 2,8,9-triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane (0.123 mL, 0.35 mmol) in Toluene (1 mL) and finally 1M LITHIUM BIS(TRIMETHYLSILYL)AMIDE (39.9 mL, 39.88 mmol) in THF was added dropwise over 1 minute. The resulting mixture was stirred at 80 °C for 18 hours. The reaction was allowed to cool to room temperature, SiO2 (23g) was added and evaporated to dryness. The crude product was purified by flash silica chromatography (120g), elution gradient 0 to 10% MeOH in EtOAc. Pure fractions were evaporated to dryness to afford 4-(4-methylpiperazin-1-yl)phenol (1.700 g, 51.0 %) as a beige solid.

출처 및 근거

ORD 기록
ord-8e16338c39aa405d9e6607bfaa8d820e
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
출처 보기

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