تفاعل #54605

ord-9889250ba2dc449bb2d7d2a9635c9889

معادلة التفاعل

C[C@H](N)C(=O)O
L-Alanine
C[C@H](NC(=O)OC(C)(C)C)C(=O)ON1C(=O)CCC1=O
Boc-Ala-OSu
CN1CCOCC1
NMM
C[C@H](NC(=O)[C@H](C)NC(=O)OC(C)(C)C)C(=O)O
Boc-Ala-Ala-OH

المتفاعلات

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىevaporated to dryness
  2. 2
    أخرىthe oily residue re-evaporated twice with DMF (30 ml each)
  3. 3
    أخرىThe salt obtained
  4. 4
    workup.ADDITIONadded, for 20 hours
  5. 5
    أخرىThe solvent was removed
  6. 6
    استخلاصThe product was extracted into EtOAc (4 times 100 ml)
  7. 7
    غسيلwashed twice with a small volume of H2O
  8. 8
    تجفيفdried over Na2SO4
  9. 9
    أخرىevaporated to a small volume
  10. 10
    workup.ADDITIONtreated with petroleum ether until cloudiness
  11. 11
    أخرىA crystalline product formed on storage in the refrigerator overnight
  12. 12
    أخرىYield

الإجراء التجريبي

L-Alanine (3.57 g, 40 mmol) was dissolved in 18.8 ml of Triton B (40 mmol), evaporated to dryness, and the oily residue re-evaporated twice with DMF (30 ml each). The salt obtained was stirred with 11.45 g of Boc-Ala-OSu (40 mmol) in 40 ml DMF, with 4 ml of NMM added, for 20 hours. The solvent was removed and the residue taken up in 10% HOAc (100 ml). The product was extracted into EtOAc (4 times 100 ml), washed twice with a small volume of H2O, dried over Na2SO4, evaporated to a small volume, and treated with petroleum ether until cloudiness developed. A crystalline product formed on storage in the refrigerator overnight: Yield, 8.2 g (76.3%); mp 115°-118°.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04148788uspto-grants-1979_04