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Sodium Hydroxide → 6-fluoro-3,4-dihydro-4-(hydroxymethyl)-2H-benzopyran-4-carboxylic acid

HRID 2248285
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반응식

HRID 2248285 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH2:9][CH2:8][C:7]([CH2:15][OH:16])([C:11]([O:13]C)=[O:12])[C:6]=2[CH:17]=1.[OH-].[Na+]>C(Cl)Cl.CCOCC>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH2:9][CH2:8][C:7]([CH2:15][OH:16])([C:11]([OH:13])=[O:12])[C:6]=2[CH:17]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 14986537Methyl 6-fluoro-3,4-dihydro-4-(hydroxymethyl)-2H-benzopyran-4-carboxylate

생성물 1

HCID 149865386-fluoro-3,4-dihydro-4-(hydroxymethyl)-2H-benzopyran-4-carboxylic acid수율 41.2%

시약·촉매·용매 1

HCID 21881112Ethyl ether methylene chloride용매

실험 절차

To a solution of 7 g (0.029 mole) Methyl 6-fluoro-3,4-dihydro-4-(hydroxymethyl)-2H-benzopyran-4-carboxylate in 200 mL of McOH was added 7.2 mL of 5N NaOH. The reaction was heated on a steam bath overnight then cooled to room temperature. The MeOH was evaporated and the residue dissolved in water then acidified to pH 4.0 with concentrated HCl. The aqueous was extracted with EtOAc and the EtOAc layer was dried over Na2SO4, filtered and evaporated to give 6 g of crude product. Chromatography on 160 g of silica gel eluting with CH2Cl2 /ether gave 2.7 g of product, m.p. 134°-135° C.

후처리

  1. temperatureThe reaction was heated on a steam bath overnight
  2. customThe MeOH was evaporated
  3. dissolutionthe residue dissolved in water
  4. extractionThe aqueous was extracted with EtOAc
  5. dry with materialthe EtOAc layer was dried over Na2SO4
  6. filtrationfiltered
  7. customevaporated
  8. customto give 6 g of crude product

출처 및 근거

ORD 기록
ord-302fe3690c844f64952203143e9f545a
출처 데이터셋
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05039672

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