2-Methylbenzoic acid → N-(3-Methoxyphenyl)-2-methylbenzene-1-carboximidic acid

HRID 1287697ノート

反応式

HRID 1287697 の反応式
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[CH3:11][O:12][C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][CH:19]=1)[NH2:16].C(N(CC)CC)C.P(Cl)(Cl)Cl>C1(C)C=CC=CC=1>[CH3:11][O:12][C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][CH:19]=1)[NH:16][C:4](=[O:6])[C:3]1[CH:7]=[CH:8][CH:9]=[CH:10][C:2]=1[CH3:1]

参加物

6

実験手順

A 13.6 g (0.1 mol) portion of o-methylbenzoic acid, 10.9 g (0.1 mol) of m-methoxyaniline and 10.1 g (0.1 mol) of triethylamine were dissolved in 250 ml of toluene. A 4.6 g (0.033 mol) amount of phosphorus trichloride was added dropwise to the above solution with stirring at 20°-60° C. After the addition, the reaction mixture was stirred at 80°-90° C for 3 hours. The reaction mixture was cooled and washed with water to remove the triethylamine hydrochloride, and the product was dried over anhydrous sodium sulfate. The toluene was removed to give 22.8 g (95%) of fine white prismatic crystals having a melting point of 142°-143° C.

後処理

  1. additionAfter the addition
  2. stirringthe reaction mixture was stirred at 80°-90° C for 3 hours
  3. temperatureThe reaction mixture was cooled
  4. washwashed with water
  5. customto remove the triethylamine hydrochloride
  6. dry with materialthe product was dried over anhydrous sodium sulfate
  7. customThe toluene was removed

出典と根拠

ORDレコード
ord-f35820833f9244fd8702dc9f84149518
出典データセット
uspto-grants-1976_10
特許番号
US03985804

反応ノート

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