Acetic Anhydride → trans-5-Methyl-3-p-nitrostyryl-1,2,4-oxadiazole

HRID 596779Notes

Reaction equation

[N+:1]([C:4]1[CH:15]=[CH:14][C:7]([CH:8]=[CH:9][C:10](=[N:12][OH:13])[NH2:11])=[CH:6][CH:5]=1)([O-:3])=[O:2].C(=O)([O-])[O-].[Na+].[Na+].[C:22](OC(=O)C)(=O)[CH3:23]>>[CH3:22][C:23]1[O:13][N:12]=[C:10](/[CH:9]=[CH:8]/[C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:15][CH:14]=2)[N:11]=1

Participants

Reactant 3

HCID 7918Acetic Anhydride

HCID 10340Sodium Carbonate

HCID 54565412p-Nitrocinnamamidoxime

Product 1

HCID 68125145trans-5-Methyl-3-p-nitrostyryl-1,2,4-oxadiazole

Procedure

A suspension of p-nitrocinnamamidoxime (20.7 g.) in acetic anhydride (70 ml.) was heated on a steam-bath for one hour when solution occurred. The cooled solution was neutralized with saturated sodium carbonate solution and the precipitated solid filtered off, washed with water, and dried. Recrystallization of the solid from ethanol (1,200 ml) gave title compound as yellow needles, 13.5g (58.5%), m.p. 190°-191°, λmax. (EtOH) 226, 310 nm., (ε 11,500, 21,000), νmax. (Nujol) 1338 and 1502 (NO2), 972 cm.-1 (trans CH=CH), τ (CF3CO2H) values include 2.15, 2.68 (AB quartet, J 17; trans CH=CH), 7.15 (CH3).

Workup

temperaturewas heated on a steam-bath for one hour when solution
filtrationthe precipitated solid filtered off
washwashed with water
customdried
customRecrystallization of the solid from ethanol (1,200 ml)

Sources & evidence

ORD record: ord-69c361d8c9ca41d497518499be5edc30
Source dataset: uspto-grants-1977_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04012377

Reaction notes

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