Ammonium Chloride → (R)-ethyl-3-azido-2-hydroxypropionate

HRID 1778601ノート

反応式

HRID 1778601 の反応式
[CH2:1]([O:3][C:4](=[O:8])[C@@H:5]1[O:7][CH2:6]1)[CH3:2].[Cl-].[NH4+].[N-:11]=[N+:12]=[N-:13].[Na+]>CN(C=O)C>[CH2:1]([O:3][C:4](=[O:8])[C@H:5]([OH:7])[CH2:6][N:11]=[N+:12]=[N-:13])[CH3:2]

参加物

5

反応条件

温度
75 °C

実験手順

Ethyl-(2R)-2,3-epoxyproprionate (0.5 g, 4.3 mmol), ammonium chloride (0.253 g, 4.73 mmol), and sodium azide (0.336 g, 5.17 mmol) were combined in DMF (8 mL), and the mixture was heated at 75° C. for 14 hours. The reaction was cooled to room temperature, and was partitioned between water and ether/hexanes (1:1 v/v). The phases were separated, and the organic phase was washed once each with water, brine, dried over MgSO4, filtered, and concentrated to an oil, which was purified by flash chromatography (silica gel/hexanes:10% ethyl acetate) to give (R)-ethyl-3-azido-2-hydroxypropionate as a clear oil (0.47 g, 2.97 mmol, 69% yield). Rf 0.27 (hexanes: 10% EtOAc, v/v, p-anisaldehyde); MS m/e [M+Na]+ calcd 182.1, found 182.0.

後処理

  1. temperatureThe reaction was cooled to room temperature
  2. customwas partitioned between water and ether/hexanes (1:1 v/v)
  3. customThe phases were separated
  4. washthe organic phase was washed once each with water, brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated to an oil, which
  8. customwas purified by flash chromatography (silica gel/hexanes:10% ethyl acetate)

出典と根拠

ORDレコード
ord-70b1c4dc310a49968fba8cca10e35bb6
出典データセット
uspto-grants-2016_02
特許番号
US09266919B2

反応ノート

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