Ethanol → ethyl N-n-octanoylanthranilate

HRID 1417864

反応式

HRID 1417864 の反応式
S(Cl)(Cl)=O.[C:5]([NH:14][C:15]1[C:16](=[CH:20][CH:21]=[CH:22][CH:23]=1)[C:17]([OH:19])=[O:18])(=[O:13])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH2:24](O)[CH3:25]>>[C:5]([NH:14][C:15]1[C:16](=[CH:20][CH:21]=[CH:22][CH:23]=1)[C:17]([O:19][CH2:24][CH3:25])=[O:18])(=[O:13])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

参加物

4

反応物 3

HCID 702EthanolHCID 24386Thionyl ChlorideHCID 41572202-(Octanoylamino)benzoic acid

生成物 1

HCID 4179835ethyl N-n-octanoylanthranilate収率 89.2%

実験手順

Thionyl chloride was dropped to ethanol and the mixture was stirred for 2 hours. Then, N-n-octanoylanthranilic acid was added to the mixture and reaction was allowed to proceed for 3 days at the room temperature. After the reaction, the solvent was removed and ethyl N-n-octanoylanthranilate was obtained from the remaining reactant after the purification by column chromatography with the yield of 89.2%.

後処理

  1. waitto proceed for 3 days at the room temperature
  2. customAfter the reaction
  3. customthe solvent was removed

出典と根拠

ORDレコード
ord-339ba06043b044979002db6ced4e7229
出典データセット
uspto-grants-1999_03
特許番号
USRE036138

関連ノート

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