تفاعل #2552

ord-15921a54043f4c95b9921819784b62d3

معادلة التفاعل

COc1ccccc1N
o-anisidine
CCN(CC)CC
triethylamine
[Na+].[OH-]
sodium hydroxide
O=C(Cl)c1ccc(CCl)cc1
4-chloromethylbenzoyl chloride
BrCC1OCCO1
2-bromomethyl-1,3-dioxolan
COc1ccccc1N(CC1OCCO1)C(=O)c1ccc(CCl)cc1
title compound
المردود 47.9%
COc1ccccc1N(CC1OCCO1)C(=O)c1ccc(CCl)cc1
4-Chloromethyl-N-(2-methoxyphenyl)-N-(1,3-dioxolan-2-yl)methylbenzamide
المردود 47.9%

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwith cooling in an ice bath
  2. 2
    workup.STIRRINGAfter 1 hour of stirring at the same temperature
  3. 3
    استخلاصthe resulting mixture was extracted with methylene chloride
  4. 4
    غسيلwashed with 10% citric acid aqueous solution and saturated brine
  5. 5
    تجفيفdried on anhydrous sodium sulfate
  6. 6
    أخرىThereafter, the solvent was removed by evaporation
  7. 7
    أخرىthe resulting residue was purified

الإجراء التجريبي

In an atmosphere of argon, a mixture consisting of o-anisidine (500 mg, 4.06 mmol), triethylamine (1.6 ml, 11.5 mmol) and 2-bromomethyl-1,3-dioxolan (0.96 ml, 8.18 mmol) was stirred at 80° C. for 4 days, dissolved in methylene chloride (8 ml) and then, with cooling in an ice bath, mixed with 20% sodium hydroxide aqueous solution (4 ml) and 4-chloromethylbenzoyl chloride (768 mg, 4.06 mmol). After 1 hour of stirring at the same temperature, the resulting mixture was extracted with methylene chloride, washed with 10% citric acid aqueous solution and saturated brine and then dried on anhydrous sodium sulfate. Thereafter, the solvent was removed by evaporation, and the resulting residue was purified by subjecting it to a silica gel column chromatography (ethyl acetate:hexane=2:5) to obtain 704 mg (47.9%) of the title compound in the form of colorless solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05728835uspto-grants-1998_03