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Lithium hydroxide, monohydrate → HCID 58155345, 화합물

HRID 1929470
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HRID 1929470 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:17])=[C:6]([C:8]2([CH:14]3[CH2:16][CH2:15]3)[CH2:12][O:11]C(=O)[NH:9]2)[CH:7]=1.O.[OH-].[Li+]>C(O)C.O>[NH2:9][C:8]([C:6]1[CH:7]=[C:2]([Br:1])[CH:3]=[CH:4][C:5]=1[F:17])([CH:14]1[CH2:16][CH2:15]1)[CH2:12][OH:11]
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참가 물질

5

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 58155231HCID 58155231, 화합물

생성물 1

HCID 58155345HCID 58155345, 화합물

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

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온도
100 °C

실험 절차

A solution of the crude (RS)-4-(5-bromo-2-fluoro-phenyl)-4-cyclopropyl-oxazolidin-2-one (4.802 g) in ethanol (25 ml) and water (125 ml) was treated with lithium hydroxide monohydrate (6.7 g, 160 mmol) and the reaction mixture was stirred at 100° C. overnight. For the workup, the reaction mixture was extracted with dichloromethane, the combined organic layers were washed with water, then dried over sodium sulfate and evaporated. The crude product was purified by chromatography on an Isolute flash NH2 column using a gradient of heptane/ethyl acetate as the eluent. (RS)-2-amino-2-(5-bromo-2-fluoro-phenyl)-2-cyclopropyl-ethanol was obtained as a yellow oil (2.27 g, 52% of theory). Mass (calculated) C11H13BrFNO [274.132]; (found) [M+H]+=274, [M+2-H]+=276.

후처리

  1. extractionFor the workup, the reaction mixture was extracted with dichloromethane
  2. washthe combined organic layers were washed with water
  3. dry with materialdried over sodium sulfate
  4. customevaporated
  5. customThe crude product was purified by chromatography on an Isolute flash NH2 column

출처 및 근거

ORD 기록
ord-9becbff5e2714d12860e427a55575f28
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08188079B2

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