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Water → HCID 58773792, 화합물

HRID 1989840
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HRID 1989840 반응식
[I:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]([O:14]CC)=[O:13])=[CH:4][CH:3]=1.O.[OH-].[Na+]>C(O)C>[I:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]([OH:14])=[O:13])=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 58773798HCID 58773798, 화합물

생성물 1

HCID 58773792HCID 58773792, 화합물수율 93%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Ethyl 6-(4-iodophenoxy)hexanoate (3.62 g, 10 mmol), in ethanol (30 ml), water (30 ml) was treated with sodium hydroxide (1 g, 25 mmol) and the reaction was stirred under reflux for 3 h. The reaction was then allowed to cool and concentrated in vacuum to a solid. The solid was then treated cautiously with ethyl acetate (100 ml) and 1N hydrochloric acid (100 ml) and the reaction stirred at room temperature for 10 min. The ethyl acetate layer was separated dried over sodium sulfate and concentrated in vacuum to give a pale yellow solid (3.11 g, 9.3 mmol, 93%), δH (CDCl3) 1.48-1.82 (6H, m, 3,4,5-CH2), 2.40 (2H, t, 2-CH2), 3.91 (2H, t, 6-CH2O), 6.67 (2H, dd, 2,6-ArH), 7.53 (2H, dd, 3,5-ArH), δc (CDCl3) 24.31, 25.50, 38.75, 33.89, 82.54, 116.87, 138.14, 158.83 and 179.97

후처리

  1. temperatureunder reflux for 3 h
  2. temperatureto cool
  3. concentrationconcentrated in vacuum to a solid
  4. additionThe solid was then treated cautiously with ethyl acetate (100 ml) and 1N hydrochloric acid (100 ml)
  5. stirringthe reaction stirred at room temperature for 10 min
  6. customThe ethyl acetate layer was separated
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated in vacuum

출처 및 근거

ORD 기록
ord-4929c9af9a3446f3bb90ded685aa312a
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07642373B2

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