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Triethylamine → Benzenepropanoic acid, 4-(cyanomethyl)-, 1,1-dimethylethyl ester

HRID 1087004
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1087004
Br[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]#[N:10])=[CH:4][CH:3]=1.[C:11]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])(=[O:14])[CH:12]=[CH2:13].C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C.C(N(CC)CC)C>C(OCC)(=O)C.C([O-])(=O)C.C([O-])(=O)C.[Pd+2]>[C:16]([O:15][C:11]([CH2:12][CH2:13][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]#[N:10])=[CH:4][CH:3]=1)=[O:14])([CH3:19])([CH3:18])[CH3:17]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 8471TriethylamineHCID 15458tert-Butyl acrylateHCID 27914Benzeneacetonitrile, 4-bromo-HCID 80271Tri-o-tolylphosphine

Produkt 1

HCID 9992094Benzenepropanoic acid, 4-(cyanomethyl)-, 1,1-dimethylethyl ester

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 167845
palladium(II) acetate
Katalysator
HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

A mixture of 5 g of p-bromophenylacetonitrile, 4.6 ml of t-butyl acrylate, 57 mg of palladium diacetate, 310 mg of tri-o-tolylphosphine and 12 ml of triethylamine is refluxed for 5 hours. The reaction mixture is diluted with ethyl acetate and washed with 10% HCl and saturated sodium bicarbonate solution. After drying over magnesium sulfate the solvent is removed in vacuo. This material is dissolved in ethanol and hydrogenated over 1.1 g of 10% palladium on carbon catalyst for 3 days at 3 atmospheres pressure of hydrogen. After filtration the solvent is removed in vacuo and the residue is chromatographed on silica gel with ether/hexane (1:1) as the eluent to afford p-(2-t-butoxycarbonyl-ethyl)-phenylacetonitrile; 2.8 g of this product is dissolved in 90 ml of tetrahydrofuran and 50 ml of methanol and to this is added 6.2 g of cobalt chloride in 90 ml of water followed by 2.1 g of sodium borohydride in small portions. After filtration and removal of solvent, the residue is chromatographed on silica gel with 7.5% methanol saturated with ammonia in methylene chloride as the eluent to afford p-(2-t-butoxycarbonyl-ethyl)-2-phenethylamine as an oil.

Aufarbeitung

  1. temperatureis refluxed for 5 hours
  2. washwashed with 10% HCl and saturated sodium bicarbonate solution
  3. dry with materialAfter drying over magnesium sulfate the solvent
  4. customis removed in vacuo
  5. dissolutionThis material is dissolved in ethanol
  6. filtrationAfter filtration the solvent
  7. customis removed in vacuo
  8. customthe residue is chromatographed on silica gel with ether/hexane (1:1) as the eluent

Quellen und Nachweise

ORD-Eintrag
ord-f9c49a890ecb4ce2a58807e503741ad5
Quelldatensatz
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05034381

Notizen zur Reaktion

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