Ammonia → 3,5-Ditert-butyl-4-hydroxybenzamide

HRID 618508

Reaktionsgleichung

Reaktionsgleichung von HRID 618508
[CH3:1][C:2]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:13]=1[OH:14])[C:8](O)=[O:9])([CH3:4])[CH3:3].C(N1C=CN=C1)([N:21]1C=CN=C1)=O.N>O1CCCC1>[CH3:1][C:2]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:13]=1[OH:14])[C:8]([NH2:21])=[O:9])([CH3:4])[CH3:3]

Komponenten

5

Edukt 3

HCID 222AmmoniaHCID 150073,5-Di-tert-butyl-4-hydroxybenzoic acidHCID 682631,1'-Carbonyldiimidazole

Produkt 1

HCID 6165023,5-Ditert-butyl-4-hydroxybenzamideAusbeute 104,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
26 °C

Versuchsvorschrift

In a 22 L Morton flask, 749 g (3.0 mol) of 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzoic acid, 533 g (3.3 mol) carbonyldiimidazole and tetrahydrofuran (THF) were combined and heated slowly to reflux and allowed to reflux for 2.5 hours. The reaction mixture was cooled to 26° C. and concentrated aqueous ammonia was added. Stirring was continued for 2 hours and the reaction mixture was allowed to stand overnight. The contents were transferred to a flask and rinsed with tetrahydrofuran (250 mL). The mixture was stirred, layers were separated, and the aqueous layer was saved. The organic layer was washed with brine (2.5 L) followed by brine/deionized (DI) water (1 L/1.5 L). The organic layer was washed with 9.7 M hydrochloric acid (HCl)/deionized water (0.25 L/2.25 L), followed by 9.7 M hydrochloric acid/deionized water (0.5 L/2.8 L), and 9.7 M hydrochloric acid/deionized water/brine (0.5 L/1.5 L/1.5 L). The organic layer was set aside while the combined aqueous layers were washed with tetrahydrofuran. The combined organic layers were washed with brine, dried with sodium sulfate (855 g) and filtered. The filtrate was evaporated to 1011 g of a wet (water), white solid. Methylene chloride was added and removed in vacuo. This procedure was repeated with ethyl acetate (6 L, then 2 L) to produce a solid residue (779 g). The residue was slurried in ethyl acetate and heptane, filtered, and dried in a vacuum oven to yield the desired amide (736 g, 98.7%) as a white solid

Aufarbeitung

  1. temperatureheated slowly
  2. temperatureto reflux
  3. temperatureto reflux for 2.5 hours
  4. waitto stand overnight
  5. customThe contents were transferred to a flask
  6. washrinsed with tetrahydrofuran (250 mL)
  7. stirringThe mixture was stirred
  8. customlayers were separated
  9. washThe organic layer was washed with brine (2.5 L)
  10. washThe organic layer was washed with 9.7 M hydrochloric acid (HCl)/deionized water (0.25 L/2.25 L)
  11. washwere washed with tetrahydrofuran
  12. washThe combined organic layers were washed with brine
  13. dry with materialdried with sodium sulfate (855 g)
  14. filtrationfiltered
  15. customThe filtrate was evaporated to 1011 g of a wet (water), white solid
  16. additionMethylene chloride was added
  17. customremoved in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-339a98be89f14a9a80b9686b6c7b6ce4
Quelldatensatz
uspto-grants-1999_09
Patentnummer
US05952360

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