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Chloroacetonitrile → 2-(3-Methoxyiminopyrrolidin-1-yl)-2-iminoethylchloride hydrochloride

HRID 622419
ノート
印刷プレビュー

反応式

HRID 622419 の反応式
[Cl:1][CH2:2][C:3]#[N:4].[Na].Cl.[CH3:7][O:8][N:9]=[C:10]1[CH2:14][CH2:13][NH:12][CH2:11]1>CO>[ClH:1].[CH3:7][O:8][N:9]=[C:10]1[CH2:14][CH2:13][N:12]([C:3](=[NH:4])[CH2:2][Cl:1])[CH2:11]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 3

HCID 7856ChloroacetonitrileHCID 5360545SodiumHCID 867424283-Methoxyiminopyrrolidine hydrochloride

生成物 1

HCID 867424272-(3-Methoxyiminopyrrolidin-1-yl)-2-iminoethylchloride hydrochloride

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

0.63 ml of chloroacetonitrile was added to a solution of 23 mg of metallic sodium in 4 ml of absolute methanol, the mixture was stirred at room temperature for about 30 minutes, then 1.5 g of 3-methoxyiminopyrrolidine hydrochloride were added and the resulting mixture stirred for a further 2 hours. After completion of the reaction, the solvent was distilled off and the concentrate mixed with anhydrous ether. The crystals which separated out were collected by filtration and washed with ether, giving 2.2 g of 2-(3-methoxyiminopyrrolidin-1-yl)-2-iminoethylchloride hydrochloride.

後処理

  1. stirringthe resulting mixture stirred for a further 2 hours
  2. customAfter completion of the reaction
  3. distillationthe solvent was distilled off
  4. additionthe concentrate mixed with anhydrous ether
  5. customThe crystals which separated out
  6. filtrationwere collected by filtration
  7. washwashed with ether

出典と根拠

ORDレコード
ord-756d2cb4878d46e4a6c00d0a0fdbe11e
出典データセット
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04771046

反応ノート

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