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Butyl iodide → HCID 20188685、化合物

HRID 1789121
ノート
印刷プレビュー

反応式

HRID 1789121 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:15]=[CH:16][CH:17]=1)[CH2:5][N:6]([CH2:11][CH2:12][CH2:13][CH3:14])[CH2:7][CH2:8][CH2:9][CH3:10].[CH2:18]([I:22])[CH2:19][CH2:20][CH3:21]>C(#N)C>[I-:22].[CH2:7]([N+:6]([CH2:5][C:4]1[CH:15]=[CH:16][CH:17]=[C:2]([OH:1])[CH:3]=1)([CH2:18][CH2:19][CH2:20][CH3:21])[CH2:11][CH2:12][CH2:13][CH3:14])[CH2:8][CH2:9][CH3:10]
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 10962Butyl iodideHCID 201886883-[(Dibutylamino)methyl]phenol

生成物 1

HCID 20188685HCID 20188685、化合物

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

A mixture was prepared containing 10 g (0.042 m) of 3-hydroxy N,N-dibutylbenzylamine, 15 g (0.082 m) of butyliodide and 25 ml of acetonitrile. The mixture was heated to reflux overnight. The completion of the reaction was determined by high pressure liquid chromatography. After completion, the solvent was removed and the residue triturated with ether, filtered and dried. The desired N,N,N-tributyl-(3-hydroxybenzyl)ammonium iodide product was recovered as a white powder in a yield of 15.7 g. The product melted at 128° C.-130° C. and its elemental analysis is as follows:

後処理

  1. customA mixture was prepared
  2. temperatureThe mixture was heated
  3. temperatureto reflux overnight
  4. customAfter completion, the solvent was removed
  5. customthe residue triturated with ether
  6. filtrationfiltered
  7. customdried
  8. customThe desired N,N,N-tributyl-(3-hydroxybenzyl)ammonium iodide product was recovered as a white powder in a yield of 15.7 g

出典と根拠

ORDレコード
ord-8a6119e32beb49ab984ec47353dcc123
出典データセット
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04687509

反応ノート

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