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Hydrochloric Acid → 4-(((1R)-2,2-difluorocyclopropyl)methoxy)benzoic Acid

HRID 2277288
ノート
印刷プレビュー

反応式

HRID 2277288 の反応式
[F:1][C:2]1([F:17])[CH2:4][C@@H:3]1[CH2:5][O:6][C:7]1[CH:16]=[CH:15][C:10]([C:11]([O:13]C)=[O:12])=[CH:9][CH:8]=1.C1COCC1.[OH-].[Na+].Cl>CO>[F:1][C:2]1([F:17])[CH2:4][C@@H:3]1[CH2:5][O:6][C:7]1[CH:16]=[CH:15][C:10]([C:11]([OH:13])=[O:12])=[CH:9][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 86731369methyl 4-(((1R)-2,2-difluorocyclopropyl)methoxy)benzoate

生成物 1

HCID 867313704-(((1R)-2,2-difluorocyclopropyl)methoxy)benzoic Acid収率 93.1%

試薬・触媒・溶媒 1

HCID 887Methanol
このページの内容参加物実験手順後処理出典と根拠反応ノート
溶媒

実験手順

A mixture of methyl 4-(((1R)-2,2-difluorocyclopropyl)methoxy)benzoate (637 mg), THF (10 mL), methanol (10 mL) and 1M aqueous sodium hydroxide solution (10 mL) was stirred at room temperature overnight. The reaction mixture was neutralized with 1M hydrochloric acid at 0° C., and the mixture was extracted with ethyl acetate. The combined organic layer were washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (559 mg).

後処理

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe combined organic layer were washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-408d12087fb94966a412ce55c2d77d92
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09133129B2

反応ノート

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