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Trifluoroacetic acid → (3RS)-3-acetoxytetradecanoic acid

HRID 2164400
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인쇄 미리보기

반응식

HRID 2164400 반응식
FC(F)(F)C(O)=O.[C:8]([O:11][CH:12]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH2:13][C:14]([O:16]C(C)(C)C)=[O:15])(=[O:10])[CH3:9]>C1C=CC=CC=1.C1(C)C=CC=CC=1>[C:8]([O:11][CH:12]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH2:13][C:14]([OH:16])=[O:15])(=[O:10])[CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6422Trifluoroacetic acidHCID 21769584Tert-butyl 3-(acetyloxy)tetradecanoate

생성물 1

HCID 14803886(3RS)-3-acetoxytetradecanoic acid수율 85.4%

시약·촉매·용매 2

HCID 241Benzene용매HCID 1140Toluene용매

실험 절차

Trifluoroacetic acid (32 ml) was added to t-butyl (3RS)-3-acetoxytetradecanoate (14 g) under ice-cooling. The mixture was stirred at the same temperature for 2 hours. The mixture was concentrated under reduced pressure to give a residue. The residue was dissolved in a mixture of benzene and toluene, and concentrated under reduced pressure to give (3RS)-3-acetoxytetradecanoic acid (10.0 g).

후처리

  1. temperaturecooling
  2. concentrationThe mixture was concentrated under reduced pressure
  3. customto give a residue
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-ecd8ab22436f4b6c8b0c4c85309815fc
출처 데이터셋
uspto-grants-1985_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04504472

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