反応 #2358574

ord-8296be7bec9643fb82d8e44d6b1c5df4

反応方程式

C=CCOC(=O)c1cccc(O)c1
Allyl 3-hydroxybenzoate
O=C(O)c1cc(OCc2ccccc2)c(OCc2ccccc2)c(OCc2ccccc2)c1
3,4,5-tribenzyloxybenzoic acid
CCN=C=NCCCN(C)C.Cl
EDC.HCl
C=CCOC(=O)c1cccc(OC(=O)c2cc(OCc3ccccc3)c(OCc3ccccc3)c(OCc3ccccc3)c2)c1
solid
収率 99.7%
C=CCOC(=O)c1cccc(OC(=O)c2cc(OCc3ccccc3)c(OCc3ccccc3)c(OCc3ccccc3)c2)c1
3-((Allyloxy)carbonyl)phenyl 3,4,5-tris(benzyloxy)benzoate
収率 99.7%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度to reflux overnight under a nitrogen atmosphere
  2. 2
    抽出The reaction was then extracted with 5% citric acid (2×), saturated aqueous sodium bicarbonate (2×), and brine (1×)
  3. 3
    乾燥dried over MgSO4
  4. 4
    ろ過filtered
  5. 5
    濃縮concentrated in vacuo

実験手順

Allyl 3-hydroxybenzoate (2.82 g, 15.8 mmol), 3,4,5-tribenzyloxybenzoic acid (10.7 g, 23.1 mmol), DMAP (5.51 g, 26.5 mmol), and CH2Cl2 (200 mL) were combined and stirred under a nitrogen atmosphere. EDC.HCl (5.51 g, 28.8 mmol) was added to the mixture and the reaction was allowed to reflux overnight under a nitrogen atmosphere. The reaction was then extracted with 5% citric acid (2×), saturated aqueous sodium bicarbonate (2×), and brine (1×), dried over MgSO4, filtered, and concentrated in vacuo to obtain a solid (9.46 g, 99%) that was used without further purification.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09120744B2uspto-grants-2015_09