تفاعل #2028900

ord-71b8de1d498949118ed3369b163e96ba

معادلة التفاعل

[BH4-].[Na+]
sodium borohydride
CCC[C@H]1CC[C@H](C(=O)CC(=O)OCC)CC1
3-oxo-3-(trans-4-propyl-cyclohexyl)-propionic acid ethyl ester
CCC[C@H]1CC[C@H](C(O)CCO)CC1
1-(trans-4-propyl-cyclohexyl)-propane-1,3-diol
المردود 73.6%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction mixture was quenched with water (1,000 ml), to which ethyl acetate (500 ml)
  2. 2
    workup.ADDITIONwas added
  3. 3
    أخرىto give two layers The water layer
  4. 4
    استخلاصwas extracted with ethyl acetate (500 ml) twice
  5. 5
    غسيلthe combined organic layer was washed with water
  6. 6
    تجفيفdried over anhydrous magnesium sulfate
  7. 7
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  8. 8
    أخرىThe residue was purified by silica gel chromatography (silica gel: 500 g, eluent: heptane/ethyl acetate=50/50 by volume)

الإجراء التجريبي

An ethanol (300 ml) solution of (3-oxo-3-(trans-4-propyl-cyclohexyl)-propionic acid ethyl ester (3) (220.0 g) prepared in the second step was added dropwise at 50° C. or lower to a suspension of sodium borohydride (45 g) in ethanol (500 ml), in a reaction vessel under an atmosphere of nitrogen, and the stirring was continued at room temperature for 5 hours. The reaction mixture was quenched with water (1,000 ml), to which ethyl acetate (500 ml) was added to give two layers The water layer was extracted with ethyl acetate (500 ml) twice, and the combined organic layer was washed with water and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (silica gel: 500 g, eluent: heptane/ethyl acetate=50/50 by volume) to give 1-(trans-4-propyl-cyclohexyl)-propane-1,3-diol (4) (135 g) in 67% yield.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08389073B2uspto-grants-2013_03