Реакция #446714

ord-e68c99d67c3e4389bcd7777e33b88a9f

Уравнение реакции

N
ammonia
Cc1ccc(N)c(C(=O)O)c1
2-amino-5-methylbenzoic acid
C1CCOC1
tetrahydrofuran
Cc1ccc(N)c(C(N)=O)c1
2-amino-5-methylbenzamide

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.WAITAfter 24 hours
  2. 2
    Концентрированиеthe mixture was concentrated under reduced pressure to a solid residue
  3. 3
    workup.DISSOLUTIONThis solid Was partially dissolved in 500 ml of dichloromethane
  4. 4
    Промывкаwashed with 200 ml of 0.1 N sodium hydroxide and 200 ml of water
  5. 5
    СушкаThe dichloromethane solution was dried
  6. 6
    Концентрированиеconcentrated to a solid Which
  7. 7
    ДругоеWas crystallized from ethyl acetate/hexane

Методика

A mixture of 15 g of 2-amino-5-methylbenzoic acid, 16 g of 1,1-carbonyldiimidazole and 500 ml of tetrahydrofuran was stirred for 2 hours at room temperature and then saturated with anhydrous ammonia with ice bath cooling. After 24 hours, 50 ml of water was added and the mixture was concentrated under reduced pressure to a solid residue. This solid Was partially dissolved in 500 ml of dichloromethane and then washed with 200 ml of 0.1 N sodium hydroxide and 200 ml of water. The dichloromethane solution was dried and concentrated to a solid Which Was crystallized from ethyl acetate/hexane, giving 3.0 g of 2-amino-5-methylbenzamide as straw-colored crystals, mp 171°-174° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05001157uspto-grants-1991_03