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Hydrochloric Acid → 5-Acetyl-4-(adamantan-1-ylmethoxy)-2-fluorobenzoic acid

HRID 1849732
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HRID 1849732 반응식
[C:1]([C:4]1[C:5]([O:15][CH2:16][C:17]23[CH2:26][CH:21]4[CH2:22][CH:23]([CH2:25][CH:19]([CH2:20]4)[CH2:18]2)[CH2:24]3)=[CH:6][C:7]([F:14])=[C:8]([CH:13]=1)[C:9]([O:11]C)=[O:10])(=[O:3])[CH3:2].O.[OH-].[Li+].Cl>O1CCCC1.O>[C:1]([C:4]1[C:5]([O:15][CH2:16][C:17]23[CH2:26][CH:21]4[CH2:20][CH:19]([CH2:25][CH:23]([CH2:22]4)[CH2:24]2)[CH2:18]3)=[CH:6][C:7]([F:14])=[C:8]([CH:13]=1)[C:9]([OH:11])=[O:10])(=[O:3])[CH3:2]
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 168937Lithium hydroxide, monohydrateHCID 86703608Methyl 5-acetyl-4-(adamantan-1-ylmethoxy)-2-fluorobenzoate

생성물 1

HCID 867036095-Acetyl-4-(adamantan-1-ylmethoxy)-2-fluorobenzoic acid수율 99.9%

시약·촉매·용매 2

HCID 962Water용매
HCID 8028
Tetrahydrofuran
용매

실험 절차

To a solution of methyl 5-acetyl-4-(adamantan-1-ylmethoxy)-2-fluorobenzoate (0.75 g, 2.10 mmol) in tetrahydrofuran (10 mL) was added a solution of lithium hydroxide monohydrate (0.441 g, 10.50 mmol) in water (4 mL) at 0° C. The reaction mixture was allowed to warm to ambient temperature and stirred for 16 hours. After adjusting the reaction mixture to pH 2 with 1 N hydrochloric acid, the mixture was extracted with ethyl acetate (3×20 mL). The combined organic phase was washed with brine (5 mL), dried over anhydrous sodium sulfate, and filtered. Concentration of the filtrate in vacuo yielded the title compound as a colorless oil (0.727 g, quant.), which was used without further purification: MS (ES−) m/z 345.3 (M−1).

후처리

  1. extractionthe mixture was extracted with ethyl acetate (3×20 mL)
  2. washThe combined organic phase was washed with brine (5 mL)
  3. dry with materialdried over anhydrous sodium sulfate
  4. filtrationfiltered

출처 및 근거

ORD 기록
ord-2c23ac96afe146388b1f07914dd0d9cf
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952169B2

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