反応 #8295

ord-e7582e27591542cc9b1ae12d23cd68f8

反応方程式

C1=CCOC1
2,5-dihydrofuran
CO
Methanol
O=N[O-].[Na+]
sodium nitrite
CCOC(=O)c1ccc(N)cc1
ethyl 4-aminobenzoate
F[B-](F)(F)F.[H+]
tetrafluoroboric acid
CCOC(=O)c1ccc(C2COC(OC)C2)cc1
title compound
CCOC(=O)c1ccc(C2COC(OC)C2)cc1
4-(5-Methoxy-tetrahydro-furan-3-yl)-benzoic acid ethyl ester

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度the mixture refluxed for 30 min
  2. 2
    ろ過The mixture is filtered through Celite® pad
  3. 3
    workup.ADDITIONthe filtrate diluted with dichloromethane (100 mL)
  4. 4
    その他The organic layer is separated
  5. 5
    濃縮concentrated in vacuo
  6. 6
    その他The residue is chromatographed on SiO2 (10% ethyl acetate/hexanes)

実験手順

A solution of sodium nitrite (1.67 g, 24.2 mmol) in water (14 mL) is added dropwise to an ice cold mixture of ethyl 4-aminobenzoate (4.0 g, 24.2 mmol) and tetrafluoroboric acid (7.8 mL, 48%, 59.78 mmol) and stirred for 30 min. Methanol (28.5 mL), 2,5-dihydrofuran (3.66 mL, 48.4 mmol) and palladium(II) acetate (70 mg, 0.31 mmol) are added and the mixture refluxed for 30 min. The mixture is filtered through Celite® pad and the filtrate diluted with dichloromethane (100 mL). The organic layer is separated and concentrated in vacuo. The residue is chromatographed on SiO2 (10% ethyl acetate/hexanes) to yield the title compound, 2.45 g (42%), as a white solid.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07087626B2uspto-grants-2006_08