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2002 33 6
Ch inese T radi tional and Herbal Drugs ·4 83·
2. 3 Ex t raction and i sola ti on: The dried pow der Hydroly si s o Ⅰ: Co mpo und Ⅰ ( 8 mg ) hy-
( 7. 25 ) 0. 5 / 2 4 ( 5 , - 2
kg was ex t ract ed t hree tim es with M eO H dro lyzed with mo l L H SO m L EtO H H O
o r t en days each tim e at roo m tem perature. A ter = 1 ∶1) in boili ng w at er ba th o r 4 h . A ter re-
rem ov al o t he so lv ent. the resi due w as suspended moval o Et O H under reduced pressure, t he mix-
2 .
in H O and successiv el y ex t ract ed with pet roleum t ure w as ex t racted with chlo ro orm th ree ti mes
( 60 ℃~ 90 ℃) , - .
et her bp Et O Ac and n Bu O H The orga ni c layer wa s eva po ra ted t o dry ness to
T he n -BuO H ex tracts ( 108 g ) w ere subject ed t o give Ⅰ a ( 5 m g) .
3
si lica gel ( CHCl -MeO H= 35 ∶1) co lum n chro- Acet ylati on o Ⅰ: Compound Ⅰ ( 2 mg ) w as
. 2 - ( 1∶2 , 0. 75 )
ma tog raphy to o bt ai n six ractio ns Fracti on six th acet ylat ed w it h Ac O py ridi ne m L at
w as ch ro mat og ra phed ov er silica g el eluted with roo m tempera ture o r 4 8 ho urs to yi eld acetat e o
CHCl3 -M eO H ( 20 ∶1) t o a o rd com po und Ⅰ Ⅰ . EI-M S ( m /z): 331, 259.
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