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

HRID 487206
ノート
印刷プレビュー

反応式

HRID 487206 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 21881112Ethyl ether methylene chloride溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-c2640519d4c043c9ac313089dcf00d0c
出典データセット
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05294635

反応ノート

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