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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Bromooctane → HCID 14745587, 화합물

HRID 1074112
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HRID 1074112 반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:4][CH:3]=1.[O-]CC.[Na+].[CH2:18](Br)[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]>C(O)C>[CH2:18]([O:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:6][CH:7]=1)[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 81401-BromooctaneHCID 28310Ethyl 4-hydroxyphenylacetateHCID 2723922Sodium ethoxide

생성물 1

HCID 14745587HCID 14745587, 화합물수율 83.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

The ethyl 4-hydroxyphenylacetate (59 g) and sodium ethoxide (22.4 g) are dissolved in ethanol (150 ml) and thereto is added n-octyl bromide (63.5 g), and the mixture is refluxed for 3 hours and concentrated under reduced pressure, and thereto is added ethyl acetate to dissolve the oily substance. The mixture is washed with water, dried over anhydrous magnesium sulfate, distilled under reduced pressure to remove ethyl acetate, and further distilled under reduced pressure to give ethyl 4-n-octyloxyphenylacetate (79.6 g, b.p. 179° C./0.1 mmHg).

후처리

  1. temperaturethe mixture is refluxed for 3 hours
  2. concentrationconcentrated under reduced pressure
  3. additionis added ethyl acetate
  4. dissolutionto dissolve the oily substance
  5. washThe mixture is washed with water
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationdistilled under reduced pressure
  8. customto remove ethyl acetate
  9. distillationfurther distilled under reduced pressure

출처 및 근거

ORD 기록
ord-a407cf90150b4e4c85c241c133eb3e71
출처 데이터셋
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04973425

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