Triethylamine hydrochloride → 3-Methyl-5-(4-nitrophenoxymethyl)-1,2,4-oxadiazole

HRID 528122Notes

Reaction equation

HRID 528122 reaction equation
[N+:1]([C:4]1[CH:14]=[CH:13][C:7]([O:8][CH2:9][C:10]([OH:12])=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].Cl.C([N:18](CC)[CH2:19][CH3:20])C.CC[N:25]=C=NCCCN(C)C.Cl.C(N(C(C)C)CC)(C)C>C1COCC1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([O:8][CH2:9][C:10]2[O:12][N:25]=[C:19]([CH3:20])[N:18]=2)=[CH:13][CH:14]=1)([O-:3])=[O:2]

Participants

6

Procedure

A mixture of 4-nitrophenoxy acetic acid (2.25 g, 11.4 mmole), acetamideoxime, triethylamine hydrochloride (3.85 g, 27.62 mmole), EDCI.HCl (4.37 g, 22.79 mmole) and diisopropylethylamine (7.42 g, 57.40 mmole) in anhydrous THF (250 ml) was refluxed for 18 h. The unhomogenous brown colored reaction mixture was quenched with water and extracted with EtOAc (3×300 mL). The combined organic layers washed successively with aqueous NaHCO3, brine and dried over anhydrous Na2SO4. Removal of solvent and purified by chromatographic purification provided 5-[(4-nitrophenoxy)methyl]-3-methyl-1,2,4-oxadiazole (1.62 g, 60%). 1H NMR (CDCl3): δ 8.24 (d, 2H, J=8.8 Hz), 7.08 (d, 2H, J=8.8 Hz), 5.36 (s, 2H), 2.44 (s, 3H).

Workup

  1. temperaturewas refluxed for 18 h
  2. customThe unhomogenous brown colored reaction mixture was quenched with water
  3. extractionextracted with EtOAc (3×300 mL)
  4. washThe combined organic layers washed successively with aqueous NaHCO3, brine
  5. dry with materialdried over anhydrous Na2SO4
  6. customRemoval of solvent
  7. custompurified by chromatographic purification

Sources & evidence

ORD record
ord-7c66173fc4ac49869007d083a01e8ca7
Source dataset
uspto-grants-2016_05
Patent number
US09346765B2

Reaction notes

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