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Hydrochloric Acid → Octyl Maleimide

HRID 885471
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 885471
[C:1]1(=[O:7])O[C:4](=[O:5])[CH:3]=[CH:2]1.[CH2:8]([NH2:16])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].C[Si](C)(C)N[Si](C)(C)C.Cl>C1C=CC=CC=1.[Zn+2].[Br-].[Br-]>[CH2:8]([N:16]1[C:4](=[O:5])[CH:3]=[CH:2][C:1]1=[O:7])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 7923Maleic AnhydrideHCID 8143OctylamineHCID 13838Hexamethyldisilazane

Produkt 1

HCID 512829Octyl MaleimideAusbeute 88 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 10421208Zinc bromide
Katalysator
HCID 241BenzeneLösungsmittel3×

Reaktionsbedingungen

Temperatur
30 °C

Versuchsvorschrift

To a suspension of maleic anhydride (54, 5.4 g, 55 mmol) in 150 ml of benzene, a solution of octyl amine (53, 6.46 g, 50 mmol) in 100 ml of benzene was added. The resulting mixture was stirred at 30° C. for an hour and ZnBr2 (12.4 g, 55 mmol) and hexamethyl disilazane (12.1 g, 75 mmol) in 30 ml of benzene were added. The resulting suspension was refluxed for 2 hrs. After cooling to room temperature, the reaction mixture was poured into 200 ml of 0.5 M HCl. The organic layer was separated and the aqueous portion was extracted twice with 150 ml portions of EtOAc. The combined organic layers were washed with saturated aqueous NaHCO3 (2×150 ml), brine (1×150 ml), and dried over Na2SO4. The solution was dried under vacuum to yield an oily product which solidified gradually to yield the cream colored solid product (9.2 g, 88%). 1H NMR (300 MHz, CDCl3): δ 0.87 (t, 3H, J=6 Hz), 1.20-1.40 (m, 10H), 1.50-1.70 (m, 2H), 3.51 (t, 2H, J=6 Hz), 6.69 (s, 2H).

Aufarbeitung

  1. temperatureThe resulting suspension was refluxed for 2 hrs
  2. temperatureAfter cooling to room temperature
  3. customThe organic layer was separated
  4. extractionthe aqueous portion was extracted twice with 150 ml portions of EtOAc
  5. washThe combined organic layers were washed with saturated aqueous NaHCO3 (2×150 ml), brine (1×150 ml)
  6. dry with materialdried over Na2SO4
  7. customThe solution was dried under vacuum
  8. customto yield an oily product which

Quellen und Nachweise

ORD-Eintrag
ord-f836df70c9fb4dd9ae8a5e55cf465066
Quelldatensatz
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08242162B2

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