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Dimethylcyanamide → HCID 178484373、化合物

HRID 635549
ノート
印刷プレビュー

反応式

HRID 635549 の反応式
Cl.[I:2][C:3]1[CH:4]=[C:5]([CH:7]=[CH:8][CH:9]=1)[NH3+:6].[CH3:10][N:11]([CH3:14])[C:12]#[N:13]>O>[I:2][C:3]1[CH:4]=[C:5]([NH:6][C:12](=[NH:13])[N:11]([CH3:14])[CH3:10])[CH:7]=[CH:8][CH:9]=1
参加物反応条件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 15112DimethylcyanamideHCID 21259554HCID 21259554、化合物

生成物 1

HCID 178484373HCID 178484373、化合物収率 81%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
130 °C

実験手順

46.00 g (0.21 mol) of 3-iodoaniline were admixed with 100 ml of 15% strength hydrochloric acid. The 3-iodoanilinium hydrochloride formed was filtered off with suction, recrystallized from water and dried under reduced pressure (yield: 52.57 g=98%). The total amount of the anilinium salt was mixed with 14.42 g (0.205 mol) of dimethylcyanamide and heated at 130° C. for 10 minutes on an oil bath. After the reaction had abated, the reaction mixture was cooled, admixed with 100 ml of water and the water-soluble constituents were filtered off. The aqueous solution was extracted twice with 100 ml each time of diethyl ether, adjusted to a pH of 10-12 using KOH and subsequently extracted three times with 100 ml of dichloromethane. The CH2Cl2 extracts were dried over magnesium sulfate and the solvent was then taken off under reduced pressure. This left 48.2 g of N′-(3-iodophenyl)-N,N-dimethylguanidine as a colorless solid (yield: 81%).

後処理

  1. filtrationwas filtered off with suction
  2. customrecrystallized from water
  3. customdried under reduced pressure (yield: 52.57 g=98%)
  4. temperaturethe reaction mixture was cooled
  5. filtrationthe water-soluble constituents were filtered off
  6. extractionThe aqueous solution was extracted twice with 100 ml each time of diethyl ether
  7. extractionsubsequently extracted three times with 100 ml of dichloromethane
  8. dry with materialThe CH2Cl2 extracts were dried over magnesium sulfate

出典と根拠

ORDレコード
ord-16e6df613e04472d91977d61ac29edfd
出典データセット
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06187953B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート