反応 #502081

ord-f321dfd592b2451ebd7ea5a593124aca

反応方程式

C(=NC1CCCCC1)=NC1CCCCC1
N,N′-dicyclohexylcarbodiimide
CC(=O)Oc1ccc2c(CC(=O)O)cc(=O)oc2c1
7-acetoxycoumarin-4-acetic acid
OCC(Cl)(Cl)Cl
2,2,2-trichloroethanol
CC(=O)Oc1ccc2c(CC(=O)OCC(Cl)(Cl)Cl)cc(=O)oc2c1
product 6a
収率 96.7%
CC(=O)Oc1ccc2c(CC(=O)OCC(Cl)(Cl)Cl)cc(=O)oc2c1
(2′,2′,2′-Trichloroethyl) 7-acetoxycoumarin-4-acetate
収率 96.7%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過filtered
  2. 2
    濃縮The filtrate was concentrated under vacuum

実験手順

To a suspension of 7-acetoxycoumarin-4-acetic acid 5 (945 mg, 3.6 mmol, 1 eq) in 47 mL of anhydrous dichloromethane at room temperature under nitrogen was added 2,2,2-trichloroethanol (431 μL, 4.5 mmol, 1.25 eq). A solution of N,N′-dicyclohexylcarbodiimide (818 mg, 4 mmol, 1.1 eq) in 10 mL of anhydrous dichloromethane was added. The reaction mixture was stirred for 15 min, after which it was diluted with dichloromethane and filtered. The filtrate was concentrated under vacuum. Column chromatography on silica gel (CH2Cl2 then CH2Cl2:EtOAc, 10:1) afforded product 6a (1.37 g, 96%): Rf 0.78 (CH2Cl2:EtOAc, 5:1); 1H NMR (300 MHz, CDCl3): δ 7.61 (d, 1H, J5,6 8.7 Hz, H-5), 7.15 (d, 1H, J6,8 2.1 Hz, H-8), 7.07 (dd, 1H, J6,8 2.3, J5,6 8.7 Hz, H-6), 6.42 (s, 1H, H-3), 4.77 (s, 2H, CH2CCl3), 3.91 (2 s, 2H, CH2CO2), 2.33 (s, 3H, OAc); 13C NMR (75 MHz, CDCl3): δ 168.6, 167.0, 154.5, 153.5, 146.5, 125.5, 118.5, 117.0, 116.5, 110.9, 74.6, 37.7, 21.2; ESI-MS: m/z 393 [M+H]+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08088745B2uspto-grants-2012_01