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Methanol → HCID 19890426, 화합물

HRID 893543
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인쇄 미리보기

반응식

HRID 893543 반응식
[OH-].[Na+].CO.[F:5][C:6]([F:27])([F:26])[CH:7]([CH2:22][CH2:23][CH2:24][CH3:25])[CH2:8][CH2:9][O:10][C:11]1[CH:21]=[CH:20][C:14]([C:15]([O:17]CC)=[O:16])=[CH:13][CH:12]=1>O>[F:5][C:6]([F:26])([F:27])[CH:7]([CH2:22][CH2:23][CH2:24][CH3:25])[CH2:8][CH2:9][O:10][C:11]1[CH:21]=[CH:20][C:14]([C:15]([OH:17])=[O:16])=[CH:13][CH:12]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 19890431HCID 19890431, 화합물

생성물 1

HCID 19890426HCID 19890426, 화합물수율 76%

시약·촉매·용매 1

HCID 962Water용매2회

반응 조건

온도
50 °C

실험 절차

0.082 g of sodium hydroxide was dissolved in 1 ml of water, followed by addition of 3 ml of methanol and 0.22 g of ethyl p-(3-trifluoromethylheptyloxy)-benzoate and 3 hours of stirring at 50° C. After the reaction, water was added, methanol was removed by distillation under a reduced pressure, and 6N-hydrochloric acid was added to precipitate a crystal. The crystal was recovered by filtration, washed with water and dried to obtain 0.15 g (yield: 76%) of p-(3-trifluoromethylheptyloxy)benzoic acid, which showed: [α]D24 +4.2, [α]43525 +8.6 (c 1.00, CHCl3).

후처리

  1. additionwas added
  2. custommethanol was removed by distillation under a reduced pressure, and 6N-hydrochloric acid
  3. additionwas added
  4. customto precipitate a crystal
  5. filtrationThe crystal was recovered by filtration
  6. washwashed with water
  7. customdried

출처 및 근거

ORD 기록
ord-483017e51de14b48b71fbca020e4acbd
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05126071

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