تفاعل #10279

ord-1a741121a16944648d852fb3d307e1e8

معادلة التفاعل

COC(CN)OC
aminoacetaldehyde dimethylacetal
O=C(Cl)CCCCCl
5-chlorovaleryl chloride
[H-].[Na+]
sodium hydride
COC(CN1CCCCC1=O)OC
1-(2,2-dimethoxyethyl)-piperidin-2-one
المردود 80.9%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe aqueous layer was separated
  2. 2
    استخلاصextracted with ethyl acetate
  3. 3
    غسيلThe combined organic phase was washed with 1% hydrochloric acid and water
  4. 4
    تجفيفdried (magnesium sulfate)
  5. 5
    تركيزconcentrated
  6. 6
    workup.DISSOLUTIONThe oily residue was dissolved in tetrahydrofuran
  7. 7
    درجة الحرارةThe reaction mixture was heated
  8. 8
    درجة الحرارةunder reflux for 1.5 hours
  9. 9
    ترشيحfiltered
  10. 10
    تركيزThe filtrate was concentrated

الإجراء التجريبي

To a stirred mixture of aminoacetaldehyde dimethylacetal (0.74 g, 7 mmole) in ethyl acetate (20 mL) and 2M sodium carbonate (20 mL) was added 5-chlorovaleryl chloride (1.55 g, 10 mmole). The reaction mixture was stirred at ambient temperature for 1 hour. The aqueous layer was separated and extracted with ethyl acetate. The combined organic phase was washed with 1% hydrochloric acid and water, dried (magnesium sulfate), and concentrated. The oily residue was dissolved in tetrahydrofuran, and sodium hydride (60% in oil) (0.3 g, 7.5 mmole) was added. The reaction mixture was heated under reflux for 1.5 hours and filtered. The filtrate was concentrated to give 1-(2,2-dimethoxyethyl)-piperidin-2-one (1.06 g) as a pale yellow oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07094778B2uspto-grants-2006_08