تفاعل #1772030

ord-cce3c7fa4b4d46e5abfd4396837c9c47

معادلة التفاعل

O=S(Cl)Cl
SOCl2
N[C@@H](CC(=O)O)C(=O)OCc1ccccc1
(S)-3-amino-4-(benzyloxy)-4-oxobutanoic acid
CO
MeOH
COC(=O)C[C@H](N)C(=O)OCc1ccccc1
(S)-1-benzyl 4-methyl 2-aminosuccinate

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةa cooled
  2. 2
    أخرىthe cooling bath was removed
  3. 3
    أخرىMost of the volatile component was removed in vacuo
  4. 4
    أخرىthe residue was carefully partitioned between EtOAc (150 mL) and saturated NaHCO3 solution
  5. 5
    استخلاصThe aqueous phase was extracted with EtOAc (150 mL, 2×)
  6. 6
    تجفيفthe combined organic phase was dried (MgSO4)
  7. 7
    ترشيحfiltered
  8. 8
    تركيزconcentrated in vacuo

الإجراء التجريبي

SOCl2 (6.60 mL, 90.5 mmol) was added drop-wise over 15 min to a cooled (ice-water) mixture of (S)-3-amino-4-(benzyloxy)-4-oxobutanoic acid (10.04 g, 44.98 mmol) and MeOH (300 mL), the cooling bath was removed and the reaction mixture was stirred at ambient condition for 29 hr. Most of the volatile component was removed in vacuo and the residue was carefully partitioned between EtOAc (150 mL) and saturated NaHCO3 solution. The aqueous phase was extracted with EtOAc (150 mL, 2×), and the combined organic phase was dried (MgSO4), filtered, and concentrated in vacuo to afford (S)-1-benzyl 4-methyl 2-aminosuccinate as a colorless oil (9.706 g). 1H NMR (DMSO-d6, δ=2.5 ppm, 400 MHz): δ 7.40-7.32 (m, 5H), 5.11 (s, 2H), 3.72 (app t, J=6.6, 1H), 3.55 (s, 3H), 2.68 (dd, J=15.9, 6.3, 1H), 2.58 (dd, J=15.9, 6.8, 1H), 1.96 (s, 2H). LC (Cond. 1): RT=0.90 min; LC/MS: Anal. Calcd. for [M+H]+ Cl2H16NO4: 238.11. found 238.22.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08147818B2uspto-grants-2012_04