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

HRID 243
ノート
印刷プレビュー

反応式

HRID 243 の反応式
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
参加物反応条件実験手順出典と根拠反応ノート

参加物

7

反応物 2

HCID 78084-BromophenolHCID 531671-Methylpiperazine

生成物 1

HCID 116224864-(4-Methyl-1-piperazinyl)phenol収率 50.99%

試薬・触媒・溶媒 4

HCID 2733832Lithium hexamethyldisilazane試薬HCID 4144353Palladium (II) acetate触媒
HCID 4571243
2,8,9-Triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo(3.3.3)undecane
触媒
HCID 1140Toluene溶媒

反応条件

温度
80 °C

実験手順

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.

出典と根拠

ORDレコード
ord-8e16338c39aa405d9e6607bfaa8d820e
出典データセット
750 AstraZeneca ELN dataset
元リンク
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反応ノート

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