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2-Methylphenyl isothiocyanate → 2-(4-Methoxy-2-o-tolylaminobenzoxazol-6-yl)acetic acid

HRID 1357861
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1357861
[NH2:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([CH2:10][C:11]([O:13]C)=[O:12])=[CH:4][C:3]=1[OH:15].[C:16]1([CH3:25])[C:17]([N:22]=[C:23]=S)=[CH:18][CH:19]=[CH:20][CH:21]=1>C(O)C>[CH3:9][O:8][C:7]1[C:2]2[N:1]=[C:23]([NH:22][C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=3[CH3:25])[O:15][C:3]=2[CH:4]=[C:5]([CH2:10][C:11]([OH:13])=[O:12])[CH:6]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 691952-Methylphenyl isothiocyanateHCID 18188079Methyl 4-amino-3-hydroxy-5-methoxy-phenylacetate

Produkt 1

HCID 181881002-(4-Methoxy-2-o-tolylaminobenzoxazol-6-yl)acetic acidAusbeute 96,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Reaktionsbedingungen

Temperatur
45 °C

Versuchsvorschrift

A mixture of methyl 4-amino-3-hydroxy-5-methoxy-phenylacetate [0.295 g, Reference Example 10(a)] and o-tolylisothiocyanate (2.14 g) in ethanol (25 mL) was left at room temperature for 3 days. The mixture was evaporated and a solution of the residue in ethanol (20 mL) was treated with dicyclohexylcarbodiimide (0.308 g). The mixture was heated at reflux temperature for 2.5 hours and then evaporated. The resulting brown oil was dissolved in methanol (30 mL) and the solution was treated with sodium hydroxide solution (10 mL, 1M) and then heated at 45° C. for one hour. The mixtures was diluted with water and then partially evaporated. The residue was washed twice with diethyl ether and the pH of the aqueous phase was adjusted to 1-2 by addition of dilute hydrochloric acid. The mixture was then extracted with ethyl acetate and the organic phase was washed with water, then with brine, then dried and then evaporated to give the title compound (0.42 g) as a golden solid.

Aufarbeitung

  1. customThe mixture was evaporated
  2. additiona solution of the residue in ethanol (20 mL) was treated with dicyclohexylcarbodiimide (0.308 g)
  3. temperatureThe mixture was heated
  4. temperatureat reflux temperature for 2.5 hours
  5. customevaporated
  6. dissolutionThe resulting brown oil was dissolved in methanol (30 mL)
  7. additionthe solution was treated with sodium hydroxide solution (10 mL, 1M)
  8. additionThe mixtures was diluted with water
  9. custompartially evaporated
  10. washThe residue was washed twice with diethyl ether
  11. additionthe pH of the aqueous phase was adjusted to 1-2 by addition of dilute hydrochloric acid
  12. extractionThe mixture was then extracted with ethyl acetate
  13. washthe organic phase was washed with water
  14. dry with materialwith brine, then dried
  15. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-3766cc6cb01245779d36c1903fabc70b
Quelldatensatz
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06593354B2

Notizen zur Reaktion

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