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Potassium Hydroxide → 10-(2-Ethylhexyloxy)decanol

HRID 1096
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HRID 1096 반응식
[CH2:1]([OH:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][OH:11].[OH-].[K+].[CH2:15]([CH:17]([CH2:20][CH2:21][CH2:22][CH3:23])[CH2:18]Br)[CH3:16]>C1(C)C(C)=CC=CC=1>[CH2:15]([CH:17]([CH2:20][CH2:21][CH2:22][CH3:23])[CH2:18][O:12][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][OH:11])[CH3:16]
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참가 물질

5

반응물 3

HCID 14797Potassium HydroxideHCID 371531,10-DecanediolHCID 868042-Ethylhexyl bromide

생성물 1

HCID 1969464710-(2-Ethylhexyloxy)decanol수율 72.1%

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

A 1-liter flask equipped with a stirrer and distiller was charged with 25 g (0.14 mol) of 1,10-decanediol, 8.09 g (0.14 mol) of KOH and 300 ml of xylene, and the resultant mixture was heated at 120° C. for 1 hour, thereby distilling off water formed. To this reaction mixture, were added 23.1 g (0.12 mol) of 2-ethylhexyl bromide, and the resulting mixture was heated and stirred for 15 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and washed with water. After the solvent was distilled off under reduced pressure, the resulting residue was purified by column chromatography on silica gel, thereby obtaining 24.8 g (yield: 72%) of 10-(2-ethylhexyloxy)decanol.

후처리

  1. customA 1-liter flask equipped with a stirrer
  2. distillationdistilling off water
  3. customformed
  4. temperaturethe resulting mixture was heated
  5. customAfter completion of the reaction
  6. washwashed with water
  7. distillationAfter the solvent was distilled off under reduced pressure
  8. customthe resulting residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-31b708e4b55e4146a82a5bb5a9af3de8
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05723497

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