تفاعل #1265354

ord-89dd5d3e10584f89a6e03d71eedf05a1

معادلة التفاعل

[Na+].[OH-]
Sodium hydroxide
O=C(Cl)OC(=O)c1ccccc1
benzoyl chloroformate
CC(C)(C)OC(=O)COCCOCCOCCOCCOCCOCCN
compound 5
CC(C)(C)OC(=O)COCCOCCOCCOCCOCCOCCN
{2-[2-(2-{2-[2-(2-Amino-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-acetic acid tert-butyl ester
CC(C)(C)OC(=O)COCCOCCOCCOCCOCCOCCNC(=O)OCc1ccccc1
compound 6
CC(C)(C)OC(=O)COCCOCCOCCOCCOCCOCCNC(=O)OCc1ccccc1
{2-[2-(2-{2-[2-(2-Benzyloxycarbonylamino-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-acetic Acid Tert-butyl Ester

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe reaction mixture was concentrated in vacuo, water (20 mL)
  2. 2
    workup.ADDITIONwas added
  3. 3
    استخلاصthe slurry was extracted with CH2Cl2 (3×100 mL)
  4. 4
    غسيلthe combined organic solutions were washed with saturated aq. NaHCO3 (20 mL) and brine (20 mL)
  5. 5
    تجفيفdried over anhydrous MgSO4
  6. 6
    تركيزThe solution was concentrated in vacuo
  7. 7
    غسيلeluted 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%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07276286B2uspto-grants-2007_10