تفاعل #54605
ord-9889250ba2dc449bb2d7d2a9635c9889
معادلة التفاعل
L-Alanine
Boc-Ala-OSu
NMM
→
Boc-Ala-Ala-OH
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىevaporated to dryness
- 2أخرىthe oily residue re-evaporated twice with DMF (30 ml each)
- 3أخرىThe salt obtained
- 4workup.ADDITIONadded, for 20 hours
- 5أخرىThe solvent was removed
- 6استخلاصThe product was extracted into EtOAc (4 times 100 ml)
- 7غسيلwashed twice with a small volume of H2O
- 8تجفيفdried over Na2SO4
- 9أخرىevaporated to a small volume
- 10workup.ADDITIONtreated with petroleum ether until cloudiness
- 11أخرىA crystalline product formed on storage in the refrigerator overnight
- 12أخرىYield
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°.