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Tetrabutylammonium Fluoride → 1-(7-Methoxybenzofuran-2-yl)-butane-1,4-diol

HRID 1282029
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HRID 1282029 반응식
[F-].C([N+](CCCC)(CCCC)CCCC)CCC.[Si]([O:26][CH2:27][CH2:28][CH2:29][CH:30]([C:32]1[O:33][C:34]2[C:40]([O:41][CH3:42])=[CH:39][CH:38]=[CH:37][C:35]=2[CH:36]=1)[OH:31])(C(C)(C)C)(C)C>>[CH3:42][O:41][C:40]1[C:34]2[O:33][C:32]([CH:30]([OH:31])[CH2:29][CH2:28][CH2:27][OH:26])=[CH:36][C:35]=2[CH:37]=[CH:38][CH:39]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 2724141Tetrabutylammonium FluorideHCID 184236524-(tert-Butyldimethylsilanyloxy)-1-(7-methoxybenzofuran-2-yl)-butan-1-ol

생성물 1

HCID 184236471-(7-Methoxybenzofuran-2-yl)-butane-1,4-diol수율 86.8%

실험 절차

Tetrabutylammonium fluoride (12 ml,1M in tetrahydrofuran) was added to a stirred solution of 4-(tert-butyldimethylsilanyloxy)-1-(7-methoxybenzofuran-2-yl)-butan-1-ol (4 g) in tetrahdrofuran (50 ml) at 0° C. After stirring cooled for 2 hours the reaction was warmed to room temperature and allowed to stir for a further 1 hour. The solvent was removed in vacuo and the residue partitioned between ethyl acetate (100 ml) and water (50 ml). The organic extract was dried over magnesium sulphate, filtered and preadsorbed onto silica. Purification by column chromatography on silica eluting with ethyl acetate yielded the title compound as a tan oil (2.34 g).

후처리

  1. temperaturecooled for 2 hours the reaction
  2. stirringto stir for a further 1 hour
  3. customThe solvent was removed in vacuo
  4. customthe residue partitioned between ethyl acetate (100 ml) and water (50 ml)
  5. extractionThe organic extract
  6. dry with materialwas dried over magnesium sulphate
  7. filtrationfiltered
  8. customPurification by column chromatography on silica eluting with ethyl acetate

출처 및 근거

ORD 기록
ord-4adcca91a5dc49b78d68efaf28ef8ce8
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06455561B1

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