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Hydroxyamine hydrochloride → 4-Pyridinecarboxaldehyde, 2,5-dichloro-, oxime

HRID 637790
ノート
印刷プレビュー

反応式

HRID 637790 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([CH:8]=O)[C:5]([Cl:10])=[CH:4][N:3]=1.Cl.[NH2:12][OH:13]>CC(O)C.Cl>[Cl:1][C:2]1[CH:7]=[C:6]([CH:8]=[N:12][OH:13])[C:5]([Cl:10])=[CH:4][N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 443297Hydroxyamine hydrochlorideHCID 27629932,5-Dichloroisonicotinaldehyde

生成物 1

HCID 1363872824-Pyridinecarboxaldehyde, 2,5-dichloro-, oxime収率 85%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid触媒HCID 3776Isopropanol溶媒

実験手順

A solution of lithium di-isopropylamide was prepared by the addition of 100 ml of 1.5 molar (M) butyllithium (in a hexane solution) to 14.2 g of di-isopropylamine in 100 ml of THF at less than -30° C. After stirring for 20 minutes the solution was cooled to below -70° C. and a solution of 20.8 g of 2,5-dichloropyridine in 56 ml of THF was added at such a rate that the temperature was maintained at below -70° C. After the addition was complete, the reaction temperature was stirred at below -70° C. for 30 minutes. A solution of 13.2 g of DMF in 30 ml THF was added at the same temperature and stirred for an additional 30 minutes. The reaction mixture was allowed to warm to room temperature then poured into a mixture containing 250 g of ice and 45 ml of concentrated HCl and stirred for 15 minutes. The acidic solution was neutralized to about pH 6-7 with 3 normal (N) NaOH. The organic layer was separated and the aqueous layer extracted with ethyl ether. The organic solutions were combined, washed with saturated NaCl solution, dried and evaporated to dryness to give about 22 g of 2,5-dichloro-4-pyridinecarboxaldehyde. This aldehyde was dissolved in 100 ml of 2-propanol, mixed with 13.8 g of hydroxylamine hydrochloride and 20 drops of concentrated HCl and heated on a steambath for 1 hour. The mixture was then poured onto 200 g of ice, stirred well and filtered leaving a solid residue. The solid was vacuum dried to give 22.8 g (85%) of the desired 2,5-dichloro-4-pyridinecarboxaldehyde oxime ##STR6##

後処理

  1. temperatureheated on a steambath for 1 hour
  2. filtrationfiltered
  3. customleaving a solid residue
  4. customdried

出典と根拠

ORDレコード
ord-93379541aead4796b5478cfa4155813a
出典データセット
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04558134

反応ノート

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