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Lithium borohydride → 2,3-Difluoro-5-methoxybenzenemethanol

HRID 1527453
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HRID 1527453 반응식
C[O:2][C:3](=O)[C:4]1[CH:9]=[C:8]([O:10][CH3:11])[CH:7]=[C:6]([F:12])[C:5]=1[F:13].[Li+].[BH4-]>C1COCC1.CCOC(C)=O>[F:13][C:5]1[C:6]([F:12])=[CH:7][C:8]([O:10][CH3:11])=[CH:9][C:4]=1[CH2:3][OH:2]
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참가 물질

5

반응물 2

HCID 4148881Lithium borohydride2회HCID 677985462,3-Difluoro-5-methoxy-benzoic acid methyl ester

생성물 1

HCID 682836852,3-Difluoro-5-methoxybenzenemethanol

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매2회HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 2,3-difluoro-5-methoxy-benzoic acid methyl ester (925 mg, 4.58 mmol) in THF (25 mL), cooled to 0° C., was added a solution of LiBH4 (199 mg, 9.15 mmol) in THF (5 mL). The reaction mixture was stirred at RT for overnight. An additional aliquot of LiBH4 (4 equiv) was added and stirring was continued at RT for 6 h, and subsequently at 60° C. overnight. The mixture was diluted with EtOAc, the organics were washed with 1N aqueous NaOH solution (50 mL), dried (Phase separator) and evaporated in vacuo to afford the title compound as a white solid. TLC Rf (c-hexane/EtOAc 1:1)=0.57; MS (LC/MS): 198.0 [M+Na]+; tR (HPLC conditions c): 3.74 min.

후처리

  1. stirringstirring
  2. waitwas continued at RT for 6 h
  3. customsubsequently at 60° C.
  4. customovernight
  5. washthe organics were washed with 1N aqueous NaOH solution (50 mL)
  6. customdried (Phase separator)
  7. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-7d0d86f219304db09219a9785990f41c
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085555B2

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