تفاعل #3592

ord-487ac92980e343ec8d41d66e51566ec1

معادلة التفاعل

O
water
CCOC(=O)c1ccc(N)cc1
ethyl 4-aminobenzoate
Cc1ccccc1C(=O)Cl
2-methylbenzoyl chloride
CCN(CC)CC
triethylamine
CCOC(=O)c1ccc(NC(=O)c2ccccc2C)cc1
ethyl 4-[(2-methylbenzoyl)amino]benzoate
المردود 76.5%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةis cooled in an ice bath
  2. 2
    workup.ADDITIONthe addition
  3. 3
    أخرىthe organic layer separated
  4. 4
    غسيلThe organic layer is washed with water, 1N HCl, 1M NaHCO3
  5. 5
    تجفيفdried over Na2SO4
  6. 6
    أخرىThe solvent is removed
  7. 7
    ترشيحthe solid slurried with ethyl acetate and filtered

الإجراء التجريبي

A mixture of 43.42 g of ethyl 4-aminobenzoate and 40.8 g of 2-methylbenzoyl chloride in 150 ml of dichloromethane is cooled in an ice bath and 26.56 g of triethylamine the solution is stirrer the addition, the solution is stirred at room temperature overnight. The mixture is poured into water and the organic layer separated. The organic layer is washed with water, 1N HCl, 1M NaHCO3 and dried over Na2SO4. The solvent is removed and the solid slurried with ethyl acetate and filtered to give 57 g of ethyl 4-[(2-methylbenzoyl)amino]benzoate as crystals, m.p. 110°-115° C. A mixture of 50.7 g of the preceding compound in 280 ml of ethyl alcohol and 55 ml of 10N NaOH is refluxed for 5 minutes. The mixture is cooled to room temperature, diluted with 200 ml of water and acidified with concentrated hydrochloric acid (pH 1-2). The mixture is filtered and the solid washed with water and dried to give 51 g of the desired product as white crystals, m.p. 270°-275° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05733905uspto-grants-1998_03