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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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4-Bromophenol → 4-Morpholinophenol

HRID 279
ノート
印刷プレビュー

反応式

HRID 279 の反応式
C1COCCN1.Oc1ccc(Br)cc1>CC(C)(C)[O-].CC(C)c1cc(C(C)C)c(-c2ccccc2P(C2CCCCC2)C2CCCCC2)c(C(C)C)c1.Cc1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.[Na+].[Pd].[Pd]>Oc1ccc(N2CCOCC2)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 8083Morpholine

生成物 1

HCID 805104-Morpholinophenol収率 31.25%

試薬・触媒・溶媒 4

HCID 23676156Sodium t-butoxide試薬HCID 9811564Bis(dibenzylideneacetone)palladium触媒
HCID 11155794
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl
触媒
HCID 1140Toluene溶媒

反応条件

温度
100 °C

実験手順

4-Bromophenol (865 mg, 5 mmol), Tris(dibenzylideneacetone)dipalladium(0) (229 mg, 0.25 mmol), 2-Dicyclohexylphosphino-2',4',6'-tri-iso-propyl-1,1'-biphenyl (238 mg, 0.50 mmol), Morpholine (0.437 mL, 5.00 mmol) and sodium tert-butoxide (1009 mg, 10.50 mmol) were stirred in toluene (5 mL) overnight at 100 °C. The mixture was allowed to cool to ambient temperature. Ethylacetate was added and the mixture was washed with aqueous NaHCO3 (satd.) and water. The organic phase was separated, dried over MgSO4, filtered and the solvent removed by rotary evaporation. The crude product was added to a silica gel column and was eluted with 0-2 % MeOH in DCM. The collected fraction were combined and the solvent was removed by rotary evaporation. 1H NMR in CDCl3 is consistent with desired product MS (m+1) = 180. HPLC Peak RT = 2.55 minutes is product. Purity = 96%.

出典と根拠

ORDレコード
ord-c3c3446fa521406ab3b5349b3ab1378a
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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