Water → HCID 178514622, compound

HRID 355233Notes

Reaction equation

HRID 355233 reaction equation
[N:1]([C@H:4]1[CH2:7][C@H:6]([C:8]([O:10]C)=[O:9])[CH2:5]1)=[N+:2]=[N-:3].O.[OH-].[Na+]>CO>[N:1]([C@H:4]1[CH2:7][C@H:6]([C:8]([OH:10])=[O:9])[CH2:5]1)=[N+:2]=[N-:3]

Participants

5

Procedure

To a solution of trans methyl 3-azidocyclobutane carboxylate (2.38 g, 15.3 mmol) in methanol (5 ml) was added water (5 ml). The resulting cloudy mixture was stirred vigorously and treated dropwise (0.5 h) with an aqueous solution of sodium hydroxide (1N, 15.3 ml) at such a rate that the temperature was kept under 25° C. The reaction mixture was stirred at 23° C. for 2 h and the methanol was evaporated in vacuo to a slightly yellow residue which was diluted with water (10 ml). The aqueous solution was washed with ether (2×10 ml), acidified with 1N hydrochloric acid and extracted with dichloromethane (4×25 ml). The organic extracts were combined, washed with water, dried over anhydrous sodium sulfate and concentrated to a colorless oil which solidified on standing; 2.02 g, 93%; mp 39°-41° C. Anal. calcd for C5H7N3O2 : C 42.55, H 5.00, N 29.78; found: C 42.41; H 5.02, N 29.59; ir (KBr) νmax : 2100 (N3) and 1705 cm-1 with shoulder at 1735 (C=O of carboxylic acid); 1Hmr (CDCl3) δ: 4.19 (1H, m, H-1) and 3.5-2.0 ppm (5H, H-2, H-3, H-4).

Workup

  1. customwas kept under 25° C
  2. stirringThe reaction mixture was stirred at 23° C. for 2 h
  3. customthe methanol was evaporated in vacuo to a slightly yellow residue which
  4. additionwas diluted with water (10 ml)
  5. washThe aqueous solution was washed with ether (2×10 ml)
  6. extractionextracted with dichloromethane (4×25 ml)
  7. washwashed with water
  8. dry with materialdried over anhydrous sodium sulfate
  9. concentrationconcentrated to a colorless oil which

Sources & evidence

ORD record
ord-43bf7d90e7aa47aaae03a2ca6005e6b7
Source dataset
uspto-grants-1983_03
Patent number
US04378314

Reaction notes

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