반응 #44000

ord-780617ed16d1496c8b8e69f04c32cc69

반응 방정식

[Na+].[OH-]
sodium hydroxide
COc1c2c(cc3ccccc13)C(=O)OC2O
3-Hydroxy-4-methoxynaphtho[2,3-c]furan-1(3H)-one
CCOC(=O)Cc1ccc(N)cc1
ethyl 4-aminophenylacetate
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
Sodium triacetoxyborohydride
CCOC(=O)Cc1ccc(N2Cc3c(cc4ccccc4c3OC)C2=O)cc1
ethyl[4-(4-methoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate
수율 54.5%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출extracted with dichloromethane (3×5 ml)
  2. 2
    기타The combined extracts were evaporated under vacuum
  3. 3
    기타the residue triturated with cyclohexane/ether

실험 절차

3-Hydroxy-4-methoxynaphtho[2,3-c]furan-1(3H)-one (50 mg, 0.22 mmol) and ethyl 4-aminophenylacetate (47 mg, 0.26 mmol) in dichloromethane (5 ml) were stirred at room temperature under nitrogen for 1 hour. Sodium triacetoxyborohydride (138 mg, 0.66 mmol) was added and stirring continued for 24 h. The reaction was adjusted to pH14 with sodium hydroxide solution (2N) and extracted with dichloromethane (3×5 ml). The combined extracts were evaporated under vacuum and the residue triturated with cyclohexane/ether to give ethyl[4-(4-methoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate as a white solid (45 mg, 54%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07732622B2uspto-grants-2010_06