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Lithium hydroxide, monohydrate → (2R)-2-({[(Phenylmethyl)oxy]amino}methyl)hexanoic acid

HRID 1396862
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HRID 1396862 반응식
[CH2:1]([C@@H:5]1[CH2:8][N:7]([O:9][CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:6]1=[O:17])[CH2:2][CH2:3][CH3:4].[OH2:18].[OH-].[Li+]>C1COCC1.CO.O>[C:11]1([CH2:10][O:9][NH:7][CH2:8][C@@H:5]([CH2:1][CH2:2][CH2:3][CH3:4])[C:6]([OH:17])=[O:18])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1
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참가 물질

5

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 16037946(3R)-1-(Benzyloxy)-3-butylazetidin-2-one

생성물 1

HCID 11694494(2R)-2-({[(Phenylmethyl)oxy]amino}methyl)hexanoic acid수율 69.2%

시약·촉매·용매 2

HCID 962Water용매HCID 21899815MeOH tetrahydrofuran용매

실험 절차

To a solution of (3R)-3-butyl-1-[(phenylmethyl)oxy]-2-azetidinone (7) (52.8 g, 0.23 mol) in THF/MeOH (3:1, 1500 mL) at 0° C. was added Lithium hydroxide monohydrate (11.4 g, 0.27 mol) in water (375 mL). The mixture was warmed up to rt and stirred overnight. TLC indicated completion of the reaction. Organic solvents were removed under vacuum, and the aqueous solution was washed with DCM, acidified with 4 N HCl to pH ˜2.0, and extracted with DCM. The extracts were dried, filtered and concentrated to provide the title compound (40 g, 69%). LCMS: (M+H)+: 252.2.

후처리

  1. customcompletion of the reaction
  2. customOrganic solvents were removed under vacuum
  3. washthe aqueous solution was washed with DCM
  4. extractionextracted with DCM
  5. customThe extracts were dried
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-bdae07fc8e4c490590daac1574a3370c
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901119B2

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