Triethylamine → Ethyl 1-(2,2-dimethylpropanoyl)piperidine-4-carboxylate

HRID 2192226

Reaktionsgleichung

Reaktionsgleichung von HRID 2192226
[NH:1]1[CH2:11][CH2:10][CH:4]([C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH2:3][CH2:2]1.C(N(CC)CC)C.[CH3:19][C:20]([CH3:25])([CH3:24])[C:21](Cl)=[O:22]>ClCCl>[C:21]([N:1]1[CH2:2][CH2:3][CH:4]([C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH2:10][CH2:11]1)(=[O:22])[C:20]([CH3:25])([CH3:24])[CH3:19]

Komponenten

5

Edukt 3

HCID 8471TriethylamineHCID 62493Pivaloyl chlorideHCID 70770Ethyl 4-piperidinecarboxylate

Produkt 1

HCID 1164515Ethyl 1-(2,2-dimethylpropanoyl)piperidine-4-carboxylateAusbeute 94 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Ethyl isonipecotate (20 mL, 130 mmol) was dissolved in 130 mL of dichloromethane and cooled to 0° C. and triethyl amine (19.9 mL, 143 mmol) was added. Trimethylacetyl chloride (16.8 mL, 136 mmol) was added dropwise and the reaction was allowed to warm to rt and stirred for 16 h. The reaction mixture was washed with hydrochloric acid solution (1.0 M, aq), sodium bicarbonate (sat., aq.) and sodium chloride (sat., aq.). The organic layer dried over magnesium sulfate, filtered and the solvent removed to provide 29.5 g (94%) of 20a as a pale orange liquid. LC-MS m/z, 242 [M+H]+.

Aufarbeitung

  1. temperatureto warm to rt
  2. washThe reaction mixture was washed with hydrochloric acid solution (1.0 M, aq), sodium bicarbonate (sat., aq.) and sodium chloride (sat., aq.)
  3. dry with materialThe organic layer dried over magnesium sulfate
  4. filtrationfiltered
  5. customthe solvent removed

Quellen und Nachweise

ORD-Eintrag
ord-a3fea73b92f849e8b0b25aec6f4d32db
Quelldatensatz
uspto-grants-2012_12
Patentnummer
US08329718B2

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