تفاعل #168342

ord-50bc3f91e9504640a225aa39a785b91e

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىquenched with saturated NH4Cl solution
  2. 2
    أخرىThe layers were separated
  3. 3
    استخلاصthe aqueous layer was extracted with EtOAc (2×10 mL)
  4. 4
    غسيلThe combined organic layers were washed with brine
  5. 5
    تجفيفdried over anhydrous Na2SO4
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    أخرىPurification of the residue on a silica gel column (0 to 50% EtOAc/hexanes)

الإجراء التجريبي

A solution of N-benzyl-2-chloro-N-((2R,3R)-2-hydroxypentan-3-yl)acetamide (210 mg, 0.7 mmol) in THF (5 mL) was added to a suspension of NaH (89 mg, 3.7 mmol) in THF (5 mL) at 0° C. The reaction mixture was stirred at 0° C. for 1 hour and then quenched with saturated NH4Cl solution. The layers were separated and the aqueous layer was extracted with EtOAc (2×10 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Purification of the residue on a silica gel column (0 to 50% EtOAc/hexanes) afforded (5R,6R)-4-benzyl-5-ethyl-6-methylmorpholin-3-one. MS APCl calc'd for C14H19NO2 [M+H]+ 234. found 234.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08846657B2uspto-grants-2014_09