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

HRID 1396859
ノート
印刷プレビュー

反応式

HRID 1396859 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

HCID 11550035(2R)-2-(hydroxymethyl)hexanoic Acid収率 107.2%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 21881883
Oxolane--water (1/1)
溶媒

反応条件

温度
0 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-2df847f0cfa5439ca0284b429c69f529
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08901119B2

反応ノート

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