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2,7-dimethyl-9H-fluorene-9-carboxylic acid → (2,7-Dimethyl-9H-fluoren-9-yl)methanol

HRID 1089842
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인쇄 미리보기

반응식

HRID 1089842 반응식
[CH3:1][C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][C:8]([CH3:15])=[CH:9][CH:10]=3)[CH:5]([C:16](O)=[O:17])[C:4]=2[CH:3]=1>C1COCC1>[CH3:1][C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][C:8]([CH3:15])=[CH:9][CH:10]=3)[CH:5]([CH2:16][OH:17])[C:4]=2[CH:3]=1
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참가 물질

3

반응물 1

HCID 3483962,7-dimethyl-9H-fluorene-9-carboxylic acid

생성물 1

HCID 348427(2,7-Dimethyl-9H-fluoren-9-yl)methanol수율 74.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 2,7-dimethyl-9-fluorenecarboxylic acid (4.3 g, 18.0 mmol) in THF (100 mL) was charged with 1M THF solution of BH3 -THF complex (36.0 mL, 36.0 mmol) at 0° C. The reaction mixture was stirred overnight at room temperature then quenched with water (100 mL) and HCl (3 mL). After addition of ethyl acetate (50 mL) the organic layer was separated and washed with 10% potassium carbonate solution, water, brine, dried over magnesium sulfate and evaporated to afford 2,7-dimethyl-9-fluorenemethanol (3.0 g, 74.4%).

후처리

custom
then quenched with water (100 mL) and HCl (3 mL)
  • additionAfter addition of ethyl acetate (50 mL) the organic layer
  • customwas separated
  • washwashed with 10% potassium carbonate solution, water, brine
  • dry with materialdried over magnesium sulfate
  • customevaporated
  • 출처 및 근거

    ORD 기록
    ord-8a1659f12a6445a09c3581eb3121e6bc
    출처 데이터셋
    uspto-grants-1992_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05079260

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