تفاعل #1265354
ord-89dd5d3e10584f89a6e03d71eedf05a1
معادلة التفاعل
Sodium hydroxide
benzoyl chloroformate
compound 5
{2-[2-(2-{2-[2-(2-Amino-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-acetic acid tert-butyl ester
→
compound 6
{2-[2-(2-{2-[2-(2-Benzyloxycarbonylamino-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-acetic Acid Tert-butyl Ester
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1تركيزThe reaction mixture was concentrated in vacuo, water (20 mL)
- 2workup.ADDITIONwas added
- 3استخلاصthe slurry was extracted with CH2Cl2 (3×100 mL)
- 4غسيلthe combined organic solutions were washed with saturated aq. NaHCO3 (20 mL) and brine (20 mL)
- 5تجفيفdried over anhydrous MgSO4
- 6تركيزThe solution was concentrated in vacuo
- 7غسيلeluted with CH2Cl2:MeOH 100:1 to 10:1 (v/v)
الإجراء التجريبي
Sodium hydroxide (2.0 mL of a 3M in water, 6.0 mmol) and benzoyl chloroformate (0.52 mL, 0.36 mmol) were added in portions to compound 5 (0.90 g, 2.3 mmol) in ethyl acetate (10 mL) and the resulting mixture was stirred overnight. The reaction mixture was concentrated in vacuo, water (20 mL) was added, and the slurry was extracted with CH2Cl2 (3×100 mL), and the combined organic solutions were washed with saturated aq. NaHCO3 (20 mL) and brine (20 mL), and dried over anhydrous MgSO4. The solution was concentrated in vacuo and the residue was loaded onto a silica gel gravity column (100 g) and eluted with CH2Cl2:MeOH 100:1 to 10:1 (v/v) to afford compound 6 as a colorless oil (0.93 g, 76%).