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Tetrabutylammonium Fluoride → (R)-2-Hydroxymethyl-8-methoxy-chroman

HRID 47949
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HRID 47949 반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:12]=1[O:11][C@@H:10]([CH2:13][O:14][Si](C(C)(C)C)(C)C)[CH2:9][CH2:8]2.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:12]=1[O:11][C@@H:10]([CH2:13][OH:14])[CH2:9][CH2:8]2
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참가 물질

4

반응물 2

HCID 2724141Tetrabutylammonium FluorideHCID 11404073tert-butyl(dimethyl)silyl [(2R)-8-methoxy-3,4-dihydro-2H-chromen-2-yl]methyl ether

생성물 1

HCID 12114956(R)-2-Hydroxymethyl-8-methoxy-chroman수율 88%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
22 °C

실험 절차

To a solution of tert-butyl(dimethyl)silyl [(2R)-8-methoxy-3,4-dihydro-2H-chromen-2-yl]methyl ether (4.50 g, 14.6 mmol) in tetrahydrofuran (150 mL) at 0° C. is added excess tetrabutylammonium fluoride (1.0 M in tetrahydrofuran) and the reaction mixture is allowed to stir at 22° C. for 30 min. The solvent is removed in vacuo and the residue is purified by flash column chromatography (silica, ethyl acetate:hexanes 1:1) to give 2.49 g (88%, 40% ee) of [(2R)-8-methoxy-3,4-dihydro-2H-chromen-2-yl]methanol as a white crystalline solid.

후처리

  1. customThe solvent is removed in vacuo
  2. customthe residue is purified by flash column chromatography (silica, ethyl acetate:hexanes 1:1)

출처 및 근거

ORD 기록
ord-e8a203b13e884966932cf2606d0b2889
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06700001B2

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