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Ethanol → 2-Chloro-6-fluorobenzylideneaminooxyacetic Acid

HRID 905370
ノート
印刷プレビュー

反応式

HRID 905370 の反応式
Cl[C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[CH:4]=O.C(O)C.[ClH:14].[C:15]([CH2:18][O:19][NH2:20])([OH:17])=[O:16].C(CON)(O)=O.C([O-])(=O)C.[Na+]>O>[Cl:14][CH:18]([O:19][N:20]=[CH:4][C:3]1[C:6]([F:10])=[CH:7][CH:8]=[CH:9][CH:2]=1)[C:15]([OH:17])=[O:16]
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 678472-Chloro-6-fluorobenzaldehydeHCID 517045Sodium AcetateHCID 2723609Aminooxyacetic acid hemihydrochloride

生成物 1

HCID 1317133292-Chloro-6-fluorobenzylideneaminooxyacetic Acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A warm solution of 2.0 gm. (0.013 mole) of 2-chloro-6-fluorobenzaldehyde in 40 ml. of ethanol was stirred into a warm solution of 1.4 gm. (0.013 equiv.) of carboxymethoxylamine hemihydrochloride and 0.6 gm. (0.007 mole) of anhyd. sodium acetate in 40 ml. of water. The mixture was heated a half-hour on the steam bath, and was then evaporated to dryness under reduced pressure to yield an oil, which was induced to crystallize by vigorous stirring. The solid material was triturated under water, removed by filtration, washed with water and dried in air to obtain 2.7 gm. (92.5%) of crude product melting from 95°-115° C. Recrystallization from n-heptaine/isopropyl alcohol gave 2.0 gm. of product melting at 116°-118° C.

後処理

  1. temperatureThe mixture was heated a half-hour on the steam bath
  2. customwas then evaporated to dryness under reduced pressure
  3. customto yield an oil, which
  4. customto crystallize by vigorous stirring
  5. customThe solid material was triturated under water
  6. customremoved by filtration
  7. washwashed with water
  8. customdried in air
  9. customto obtain 2.7 gm
  10. custommelting from 95°-115° C
  11. customRecrystallization from n-heptaine/isopropyl alcohol
  12. customgave 2.0 gm

出典と根拠

ORDレコード
ord-355e24221fb747d4a80019e3eea9bb25
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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