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Butyl iodide → HCID 20188685, 화합물

HRID 1789121
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HRID 1789121 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10962Butyl iodideHCID 201886883-[(Dibutylamino)methyl]phenol

생성물 1

HCID 20188685HCID 20188685, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

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:

후처리

  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

출처 및 근거

ORD 기록
ord-8a6119e32beb49ab984ec47353dcc123
출처 데이터셋
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04687509

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