反応 #1778

ord-c76a22e184294ef893b6fc5df9e611d7

反応方程式

OC1CCOc2ccccc21
4-chromanol
CCOC(=O)N=NC(=O)OCC
diethyl azodicarboxylate
COC(=O)c1ccc(O)cc1OC
methyl 4-hydroxy-2-methoxybenzoate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
COC(=O)c1ccc(OC(=O)C2CCOc3ccccc32)cc1OC
methyl 4-(4-chromanoyloxy)-2-methoxybenzoate

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The reaction was filtered
  2. 2
    その他the solvent was removed under reduced pressure
  3. 3
    その他The residue was chromatographed on a silica gel column
  4. 4
    洗浄EtOAc and eluted with same
  5. 5
    その他the solvent removed under reduced pressure

実験手順

To a stirred solution of methyl 4-hydroxy-2-methoxybenzoate (364 mg, 2.0 mmol) in dry THF (1.25 mL) was added triphenylphosphine (525 mg, 2.0 mmol) and the solution was cooled to 0° C. A 500 mL volume of 4-chromanol (200 mg, 1.33 mmol) and diethyl azodicarboxylate (315 mL, 2.0 mmol) in THF was added dropwise via syringe over 0.5 h. The reaction was filtered and the solvent was removed under reduced pressure. The residue was chromatographed on a silica gel column packed in 92:8 hexanes:EtOAc and eluted with same. The appropriate fractions were combined and the solvent removed under reduced pressure to afford methyl 4-(4-chromanoyloxy)-2-methoxybenzoate.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05726172uspto-grants-1998_03