5-Aminovaleric acid → HCID 19808302, compound

HRID 1659519Notes

Reaction equation

HRID 1659519 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]([OH:8])=[O:7].CN(C)C(=N)N(C)C.[C:17]([O:21][C:22](N=[N+]=[N-])=[O:23])([CH3:20])([CH3:19])[CH3:18]>CN(C)C=O>[C:17]([O:21][C:22]([CH:5]([CH2:4][CH2:3][CH2:2][NH2:1])[C:6]([OH:8])=[O:7])=[O:23])([CH3:20])([CH3:19])[CH3:18]

Participants

5

Procedure

5-Amino pentanoic acid (0.585 g, 5 m mol) was stirred for two days in dimethylformamide (5 ml) containing tetramethylguanidine (1.14 g, 10 m mol) and tert.butoxycarbonylazide (1.1 g, 7.5 m mol). The solution was evaporated and the residue partitioned between ethyl acetate (20 ml) and 10% citric acid solution (20 ml). The organic layer was washed with 10% citric acid (2×15 ml), water (3×15 ml) and brine 1×15 ml). Each aqueous wash was back extracted with ethyl acetate (20 ml). The combined organic layers were dried over anhydrous magnesium sulphate and evaporated to give an oil which slowly crystallised. Recrystallisation from diisopropyl ether/petrol gave 0.745 g (70% yield), mp. 47.5°-48.5° C., Rf silica gel 0.40 (benzene:dioxan:acetic acid 95:75:4).

Workup

  1. customThe solution was evaporated
  2. customthe residue partitioned between ethyl acetate (20 ml) and 10% citric acid solution (20 ml)
  3. washThe organic layer was washed with 10% citric acid (2×15 ml), water (3×15 ml) and brine 1×15 ml)
  4. washEach aqueous wash
  5. extractionwas back extracted with ethyl acetate (20 ml)
  6. dry with materialThe combined organic layers were dried over anhydrous magnesium sulphate
  7. customevaporated
  8. customto give an oil which
  9. customslowly crystallised
  10. customRecrystallisation from diisopropyl ether/petrol
  11. customgave 0.745 g (70% yield), mp. 47.5°-48.5° C., Rf silica gel 0.40 (benzene:dioxan:acetic acid 95:75:4)

Sources & evidence

ORD record
ord-d2873f96791e4c92bdbf0021b8b14725
Source dataset
uspto-grants-1981_12
Patent number
US04304715

Reaction notes

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