Ammonia → 2-Amino-5-methylbenzamide

HRID 359532

反応式

HRID 359532 の反応式
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([CH3:11])=[CH:7][C:3]=1[C:4](O)=[O:5].O1CCCC1.[NH3:17]>O>[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([CH3:11])=[CH:7][C:3]=1[C:4]([NH2:17])=[O:5]

参加物

5

実験手順

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.

後処理

  1. waitAfter 24 hours
  2. concentrationthe mixture was concentrated under reduced pressure to a solid residue
  3. dissolutionThis solid Was partially dissolved in 500 ml of dichloromethane
  4. washwashed with 200 ml of 0.1 N sodium hydroxide and 200 ml of water
  5. dry with materialThe dichloromethane solution was dried
  6. concentrationconcentrated to a solid Which
  7. customWas crystallized from ethyl acetate/hexane

出典と根拠

ORDレコード
ord-e68c99d67c3e4389bcd7777e33b88a9f
出典データセット
uspto-grants-1991_03
特許番号
US05001157

関連ノート

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