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Sodium Hydroxide → HCID 20206318, compound

HRID 355246
Notes
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Reaction equation

HRID 355246 reaction equation
[N:1]([CH:4]([CH2:10][CH2:11][CH3:12])[C:5]([O:7]CC)=[O:6])=[N+:2]=[N-:3].[OH-].[Na+]>CO.O>[N:1]([CH:4]([CH2:10][CH2:11][CH3:12])[C:5]([OH:7])=[O:6])=[N+:2]=[N-:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 14798Sodium HydroxideHCID 23448170HCID 23448170, compound

Product 1

HCID 20206318HCID 20206318, compoundYield 93%

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 962WaterSolvent

Procedure

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 combined 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: 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.

Workup

  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 combined 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)

Sources & evidence

ORD record
ord-6c7727172141485987f66f592530f064
Source dataset
uspto-grants-1983_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04378314

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes