Methyl 3-aminocrotonate → HCID 10669204, compound

HRID 622730Notes

Reaction equation

HRID 622730 reaction equation
[C:1]([C:4](=[CH:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([N+:19]([O-:21])=[O:20])[CH:14]=1)[C:5]([O:7][CH:8]([CH3:11])[CH2:9][Cl:10])=[O:6])(=O)[CH3:2].[NH2:22]/[C:23](/[CH3:29])=[CH:24]\[C:25]([O:27][CH3:28])=[O:26]>C(O)(C)C.C(OCC)C>[CH3:29][C:23]1[NH:22][C:1]([CH3:2])=[C:4]([C:5]([O:7][CH:8]([CH3:11])[CH2:9][Cl:10])=[O:6])[CH:12]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([N+:19]([O-:21])=[O:20])[CH:14]=2)[C:24]=1[C:25]([O:27][CH3:28])=[O:26]

Participants

5

Reactant 2

HCID 643918Methyl 3-aminocrotonateHCID 53673654HCID 53673654, compound

Product 1

HCID 10669204HCID 10669204, compoundYield 64.1%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 3776IsopropanolSolvent

Procedure

A solution comprising 18.72 g of 1-methyl-2-chloroethyl α-acetyl-3-nitrocinnamate, prepared as described in Example 1, and 7.12 g of methyl 3-aminocrotonate in 48 ml of isopropanol was refluxed under stirring for 210 minutes. After cooling, the reaction mixture was evaporated to dryness under vacuum and the oil thus obtained was chromatographed on silica gel (200 g) using chloroform as eluent. Evaporating the fractions containing a sole product (TLC, chloroform:ethylacetate 95:5) gave a thick oil, which was dissolved in diethyl ether. The solvent was then evaporated off at 20°-25° C. to give 15.75 g of the title compound, m.p. 95°-102° C., which could be employed without further purification.

Workup

  1. customprepared
  2. temperaturewas refluxed
  3. temperatureAfter cooling
  4. customthe reaction mixture was evaporated to dryness under vacuum
  5. customthe oil thus obtained
  6. customwas chromatographed on silica gel (200 g)
  7. customEvaporating the fractions
  8. additioncontaining a sole product (TLC, chloroform:ethylacetate 95:5)
  9. customgave a thick oil, which
  10. customThe solvent was then evaporated off at 20°-25° C.

Sources & evidence

ORD record
ord-17d82d38e98142358120f90c0ffaa4a4
Source dataset
uspto-grants-1988_09
Patent number
US04772621

Reaction notes

Loading…