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Ethanol → 2,3,6-Trichlorobenzylideneaminooxyacetic Acid

HRID 905368
ノート
印刷プレビュー

反応式

HRID 905368 の反応式
Cl[C:2]1[C:9]([Cl:10])=[CH:8][CH:7]=[C:6]([Cl:11])[C:3]=1[CH:4]=O.C(O)C.[ClH:15].[C:16]([CH2:19][O:20][NH2:21])([OH:18])=[O:17].C(CON)(O)=O.C([O-])(=O)C.[Na+]>O>[Cl:15][CH:19]([O:20][N:21]=[CH:4][C:3]1[C:6]([Cl:11])=[CH:7][CH:8]=[C:9]([Cl:10])[CH:2]=1)[C:16]([OH:18])=[O:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 702EthanolHCID 207812,3,6-TrichlorobenzaldehydeHCID 517045Sodium AcetateHCID 2723609Aminooxyacetic acid hemihydrochloride

生成物 1

HCID 1317133272,3,6-Trichlorobenzylideneaminooxyacetic Acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A warm solution of 3.0 gm. (0.014 mole) of 2,3,6-trichlorobenzaldehyde in 50 ml. of ethanol was stirred into a warm solution of 1.6 gm. (0.015 equiv.) of carboxymethoxylamine hemihydrochloride and 0.7 gm. (0.008 mole) of anhyd. sodium acetate in 50 ml. water. Heating on the steam bath was maintained for one-half hour: then the reaction mixture was evaporated by 3/4 volume and was cooled. The solid present was removed by filtration, washed with water and dried in vacuum dessicator over phosphorus pentoxide to obtain 3.9 gm. (96.5%) of crude product melting at 159°-160° C. This material, twice recrystallized from aqueous-isopropyl alcohol, melted at 160°-161° C.

後処理

  1. temperatureHeating on the steam bath
  2. temperaturewas maintained for one-half hour
  3. customthe reaction mixture was evaporated by 3/4 volume
  4. temperaturewas cooled
  5. customThe solid present was removed by filtration
  6. washwashed with water
  7. dry with materialdried in vacuum dessicator over phosphorus pentoxide
  8. customto obtain 3.9 gm
  9. customThis material, twice recrystallized from aqueous-isopropyl alcohol, melted at 160°-161° C.

出典と根拠

ORDレコード
ord-5e8111f1141546d2afe8d8ea6c8beaef
出典データセット
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04423241

反応ノート

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