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

HRID 2277288
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HRID 2277288 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol
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실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-408d12087fb94966a412ce55c2d77d92
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133129B2

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