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Dichloroacetyl chloride → N-dichloroacetylpiperid-4-one ethylene ketal

HRID 65387
ノート
印刷プレビュー

反応式

HRID 65387 の反応式
[Cl:1][CH:2]([Cl:6])[C:3](Cl)=[O:4].[CH2:7]1[O:16][C:10]2([CH2:15][CH2:14][NH:13][CH2:12][CH2:11]2)[O:9][CH2:8]1>C1(C)C=CC=CC=1>[CH2:7]1[O:16][C:10]2([CH2:15][CH2:14][N:13]([C:3](=[O:4])[CH:2]([Cl:6])[Cl:1])[CH2:12][CH2:11]2)[O:9][CH2:8]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6593Dichloroacetyl chlorideHCID 674351,4-Dioxa-8-azaspiro(4.5)decane

生成物 1

HCID 13018227N-dichloroacetylpiperid-4-one ethylene ketal収率 49.2%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

12.4 g (0.084 mol) of dichloroacetyl chloride was added dropwise to a mixture of 12 g (0.084 mol) of piperid-4-one ethylene ketal and 12.8 g (0.084 mol) of 1,8-diazobicyclo[5.4.0]undec-7-ene in 100 ml of toluene, whilst stirring, at a rate such that the temperature of the reaction mixture did not exceed 40° C. Thereafter, the mixture was subsequently stirred at 20° C. for 2 hours. Working up was then effected by a procedure in which the reaction mixture was filtered, the filtrate was concentrated under reduced pressure and the residue was recrystallized from a mixture of toluene and petroleum ether. 10.5 g (49% of theory) of N-dichloroacetylpiperid-4-one ethylene ketal were obtained in this manner in the form of colorless crystals of melting point 102° C.

後処理

  1. customdid not exceed 40° C
  2. stirringThereafter, the mixture was subsequently stirred at 20° C. for 2 hours
  3. filtrationwas filtered
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. customthe residue was recrystallized from a mixture of toluene and petroleum ether

出典と根拠

ORDレコード
ord-8cc022afb8cb4deeb6634dc0ea0dc597
出典データセット
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04614537

反応ノート

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