تفاعل #2028899

ord-64f72b43543648c4939c1fdb8ec94732

معادلة التفاعل

[Li][CH2]CCC
n-Butyllithium
CCC[C@H]1CC[C@H](C(=O)Cl)CC1
trans-4-propylcyclohexanecarboxylic acid chloride
CCOC(C)=O
ethyl acetate
CC(C)NC(C)C
diisopropylamine
CCC[C@H]1CC[C@H](C(=O)CC(=O)OCC)CC1
3-oxo-3-(trans-4-propyl-cyclohexyl)-propionic acid ethyl ester
المردود 91.0%

المذيبات

ظروف التفاعل

درجة الحرارة
-65°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas kept at −40° C.
  2. 2
    workup.ADDITIONwere added dropwise
  3. 3
    درجة الحرارةAfter the reaction mixture had been slowly warmed up to room temperature
  4. 4
    أخرىit was quenched with a saturated aqueous solution of ammonium chloride
  5. 5
    workup.ADDITIONWater (1,000 ml) was then added
  6. 6
    أخرىto give two layers
  7. 7
    استخلاصThe water layer was extracted with toluene (500 ml) three times
  8. 8
    غسيلthe combined organic layer was washed with water
  9. 9
    تجفيفdried over anhydrous magnesium sulfate
  10. 10
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  11. 11
    أخرىThe residue was purified by silica gel chromatography (silica gel: 300 g, eluent: toluene)

الإجراء التجريبي

THF (1,000 ml) was added to diisopropylamine (162.9 g) in a reaction vessel under an atmosphere of nitrogen. n-Butyllithium was added dropwise, while the solution was kept at −40° C. or lower, and the stirring was continued for 30 minutes. The solution was cooled at −65° C. or lower, and ethyl acetate (141.9 g) and then a THF (200 ml) solution of trans-4-propylcyclohexanecarboxylic acid chloride (2) (189.9 g) prepared in the first step were added dropwise. After the reaction mixture had been slowly warmed up to room temperature with stirring, it was quenched with a saturated aqueous solution of ammonium chloride. Water (1,000 ml) was then added to give two layers. The water layer was extracted with toluene (500 ml) three times, 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: 300 g, eluent: toluene) to give 3-oxo-3-(trans-4-propyl-cyclohexyl)-propionic acid ethyl ester (3) (220 g) in 90% yield.

المصدر

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