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Sodium Hydroxide → HCID 20206318, 화합물

HRID 1680344
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HRID 1680344 반응식
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]
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 23448170HCID 23448170, 화합물

생성물 1

HCID 20206318HCID 20206318, 화합물수율 93%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-27e651ec648143d6b1d51c7c0bf5d129
출처 데이터셋
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04272437

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