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Potassium Hydroxide → (R)-4-(4-Fluoro-3-methyl-phenyl)-4-hydroxy-butanoic acid

HRID 1643263
ノート
印刷プレビュー

反応式

HRID 1643263 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([OH:15])[CH2:9][CH2:10][C:11]([O:13]C)=[O:12])=[CH:4][C:3]=1[CH3:16].[OH-].[K+]>O1CCOCC1>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([OH:15])[CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[CH:4][C:3]=1[CH3:16]
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 14797Potassium HydroxideHCID 59568813(R)-Methyl 4-(4-fluoro-3-methylphenyl)-4-hydroxybutanoate

生成物 1

HCID 42077386(R)-4-(4-Fluoro-3-methyl-phenyl)-4-hydroxy-butanoic acid

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

To a solution of (R)-Methyl 4-(4-fluoro-3-methylphenyl)-4-hydroxybutanoate (181 mg, 0.80 mmol) in 5 mL dioxane was added 5 mL aqueous 5% KOH at 25° C. The mixture was stirred for 30 min at room temperature and then the reaction quenched by the addition of 10 mL of 1M HCl and the resulting mixture extracted with ethyl acetate (2×10 mL). The combined organic layers were extracted with 5% K2CO3 (3×5 mL) and the aqueous extracts acidified with 1M HCl to pH3. The resulting white colloidal suspension was extracted with ethyl acetate (3×20 mL) and the combined organic layers washed with brine (2×15 mL) before being dried over Na2SO4. The solvent was evaporated under reduced pressure and the crude product (233 mg) was used in the next step without further purification.

後処理

  1. customthe reaction quenched by the addition of 10 mL of 1M HCl
  2. extractionthe resulting mixture extracted with ethyl acetate (2×10 mL)
  3. extractionThe combined organic layers were extracted with 5% K2CO3 (3×5 mL)
  4. extractionThe resulting white colloidal suspension was extracted with ethyl acetate (3×20 mL)
  5. washthe combined organic layers washed with brine (2×15 mL)
  6. dry with materialbefore being dried over Na2SO4
  7. customThe solvent was evaporated under reduced pressure
  8. customthe crude product (233 mg) was used in the next step without further purification

出典と根拠

ORDレコード
ord-e450c335c68e4a2782b4e80d4c507df8
出典データセット
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08119692B2

反応ノート

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