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Sodium Hydroxide → HCID 20206318、化合物

HRID 1680344
ノート
印刷プレビュー

反応式

HRID 1680344 の反応式
C([O:3][C:4](=[O:12])[CH:5]([N:9]=[N+:10]=[N-:11])[CH2:6][CH2:7][CH3:8])C.[OH-].[Na+]>CO.O>[N:9]([CH:5]([CH2:6][CH2:7][CH3:8])[C:4]([OH:12])=[O:3])=[N+:10]=[N-:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14798Sodium HydroxideHCID 23448170HCID 23448170、化合物

生成物 1

HCID 20206318HCID 20206318、化合物収率 93%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

A solution of ethyl-2-azidopentanoate (3.082 g, 18.0 mmol) in a mixture of methanol (10 ml) and water (5 ml) was treated dropwise with 20 ml of 1M sodium hydroxide (20 mmol, 1.1 equiv). After 1.5 h at room temperature, the methanol was evaporated under reduced pressure and the remaining aqueous phase was washed with ether (2×10 ml) and acidified with dilute HCl (3N) at 0° C. The aqueous phase was extracted with dichloromethane (3×25 ml). The compound organic phases were washed with water and dried over anhydrous sodium sulfate. Evaporation of the solvent gave an oil which was distilled (bulb to bulb) to give 2.393 g (93%) of a clear liquid: bp 80°-85° C./0.5 toor (air bath temperature; ir (firm) νmax : 2110 (N3), 1720 cm-1 (C=O); 1Hmr (CDCl3) δ: 3.90 (1H, dd, J=6, J=7, H-2), 2.0-1.0 (4H, m, H-3, H-4) and 1.00 ppm (3H, distorted t, J=6, H-5); Anal. calcd for C5H9N3O2 : C 41.95, H 6.34, N 29.36; found: C 42.06, H 6.49, N 29.26.

後処理

  1. customthe methanol was evaporated under reduced pressure
  2. washthe remaining aqueous phase was washed with ether (2×10 ml)
  3. customacidified with dilute HCl (3N) at 0° C
  4. extractionThe aqueous phase was extracted with dichloromethane (3×25 ml)
  5. washThe compound organic phases were washed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. customEvaporation of the solvent
  8. customgave an oil which
  9. distillationwas distilled (bulb to bulb)

出典と根拠

ORDレコード
ord-27e651ec648143d6b1d51c7c0bf5d129
出典データセット
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04272437

反応ノート

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