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p-Toluenesulfonic acid → 4-(Hex-1-EN-1-YL)benzene-1,2-diol

HRID 569642
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인쇄 미리보기

반응식

HRID 569642 반응식
O1CCCCC1[O:7][C:8]1[CH:9]=[C:10]([CH:21]=[CH:22][CH2:23][CH2:24][CH2:25][CH3:26])[CH:11]=[CH:12][C:13]=1[O:14]C1CCCCO1.C1(C)C=CC(S(O)(=O)=O)=CC=1>CO.C(N(CC)CC)C>[OH:7][C:8]1[CH:9]=[C:10]([CH:21]=[CH:22][CH2:23][CH2:24][CH2:25][CH3:26])[CH:11]=[CH:12][C:13]=1[OH:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 54203799HCID 54203799, 화합물

생성물 1

HCID 534261164-(Hex-1-EN-1-YL)benzene-1,2-diol수율 57.8%

시약·촉매·용매 2

HCID 8471Triethylamine촉매HCID 887Methanol용매

실험 절차

In 10 ml of absolute methanol was dissolved 198 mg of 1-(3',4'-bistetrahydropyranyloxy-phenyl)-1-hexene obtained in Example 17-(1), and a catalytic amount of p-toluenesulfonic acid was added to the solution at 0° C. The mixture was stirred for 2 hours at the same temperature. After reaction, one drop of triethylamine was added to the reaction mixture and the mixture was concentrated to give crude product. By purification of the crude product by means of column chromatography [silica gel/ether:hexane (1:2)], 61 mg of pure product was obtained.

후처리

  1. additionwas added to the reaction mixture
  2. concentrationthe mixture was concentrated
  3. customto give crude product
  4. customBy purification of the crude product by means of column chromatography [silica gel/ether:hexane (1:2)]

출처 및 근거

ORD 기록
ord-ed314e311b6049a7876f87f064a54632
출처 데이터셋
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04733002

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