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Sodium Iodide → HCID 131712367、化合物

HRID 1577048
ノート
印刷プレビュー

反応式

HRID 1577048 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[Cl:12])[NH:5][CH2:6][CH2:7]Cl.[C:13]([NH2:17])([CH3:16])([CH3:15])[CH3:14].[I-].[Na+]>C(OCC)C>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([NH:5][CH2:6][CH2:7][NH:17][C:13]([CH3:16])([CH3:15])[CH3:14])[CH:9]=[CH:10][C:11]=1[Cl:12]
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 5238Sodium IodideHCID 6385Tert-ButylamineHCID 233170893,4-dichloro-N-(2-chloroethyl)aniline

生成物 1

HCID 131712367HCID 131712367、化合物収率 159.4%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

15.0 g of 2-(3,4-dichloroanilino)ethylchloride, 19.2 g of tert.butylamine and approximately 1 g of sodium iodide were stirred for 26 hours at 90° C. After having been left to stand the weekend over at room temperature, the product was taken up in diethyl ether, washed with successively 2 N sodium hydroxide solution and sodium bicarbonate solution and dried. After evaporating the solvent, 15.85 g of product were obtained, which were purified by column chromatography and then converted into the HCl salt with an alcoholic HCl solution. Melting point 206°-207° C.

後処理

  1. waitAfter having been left
  2. customover at room temperature
  3. washwashed with successively 2 N sodium hydroxide solution and sodium bicarbonate solution
  4. customdried
  5. customAfter evaporating the solvent

出典と根拠

ORDレコード
ord-9b740909c65a442f86d34d5b656a088a
出典データセット
uspto-grants-1981_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04286983

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート