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Hydrogen Peroxide → (2R)-2-(hydroxymethyl)hexanoic Acid

HRID 1396859
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HRID 1396859 반응식
[OH:1][CH2:2][C@@H:3]([CH2:19][CH2:20][CH2:21][CH3:22])[C:4](N1[C@@H](CC2C=CC=CC=2)COC1=O)=[O:5].[OH:23]O.O.[OH-].[Li+]>C1COCC1.O.O>[OH:1][CH2:2][C@@H:3]([CH2:19][CH2:20][CH2:21][CH3:22])[C:4]([OH:5])=[O:23]
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참가 물질

6

반응물 3

HCID 784Hydrogen PeroxideHCID 168937Lithium hydroxide, monohydrateHCID 68288061(4S)-3-[(2R)-2-(hydroxymethyl)hexanoyl]-4-(phenylmethyl)-1,3-oxazolidin-2-one

생성물 1

HCID 11550035(2R)-2-(hydroxymethyl)hexanoic Acid수율 107.2%

시약·촉매·용매 2

HCID 962Water용매
HCID 21881883
Oxolane--water (1/1)
용매

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온도
0 °C

실험 절차

To a 2000 mL roundbottom flask was added (4S)-3-[(2R)-2-(hydroxymethyl)hexanoyl]-4-(phenylmethyl)-1,3-oxazolidin-2-one (4) (82 g, 0.268 mol) in THF/water (4:1, 750 mL). The solution was cooled to 0° C. and H2O2 (130 mL, 1.07 mol) was added dropwise, followed by lithium hydroxide monohydrate (22.58 g, 0.537 mol) in water (130 mL). The reaction mixture was warmed up to rt and stirred overnight. THF was removed under vacuum, and the aqueous solution was washed with ethyl acetate. The aqueous solution was then acidified to pH ˜3.0 and extracted with ethyl acetate. The extracts were dried (Na2SO4), filtered and concentrated to provide the title compound (42 g, 107%). LCMS: (2M+H)+: 313.2.

후처리

  1. temperatureThe reaction mixture was warmed up to rt
  2. customTHF was removed under vacuum
  3. washthe aqueous solution was washed with ethyl acetate
  4. extractionextracted with ethyl acetate
  5. dry with materialThe extracts were dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2df847f0cfa5439ca0284b429c69f529
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901119B2

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