Ammonia → (2R-cis)-4-(2-aminoethyl)-1,5-dioxaspiro[5.5]undecane-2-acetic acid

HRID 360022

Reaktionsgleichung

[C:1]([CH2:3][C@H:4]1[O:9][C:8]2([CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)[O:7][C@@H:6]([CH2:15][C:16]([OH:18])=[O:17])[CH2:5]1)#[N:2].N.O.[H][H]>CO>[NH2:2][CH2:1][CH2:3][C@H:4]1[O:9][C:8]2([CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)[O:7][C@@H:6]([CH2:15][C:16]([OH:18])=[O:17])[CH2:5]1

Komponenten

Reaktionsbedingungen

Temperatur: 40 °C

Versuchsvorschrift

A solution of 0.13 g of (±)-cis-4-(cyanomethyl)-1,5-dioxaspiro[5.5]undecane-2-acetic acid in 20 mL of methanol saturated with anhydrous ammonia is added to a Parr shaker bottle containing 0.2 g of water wet Raney nickel #30. The solution is heated at 40° C. and 50 pounds per square inch gage (psig) hydrogen pressure for 17 hours. The suspension is cooled and filtered to remove the Raney nickel through filter aid and the precipitate is washed with methanol. The filtrate is concentrated at reduced pressure. The residue is dissolved in methanol saturated with anhydrous ammonia, treated with decolorizing charcoal, filtered through filter aid and evaporated to give 0.13 g of (±)-cis-4-(2-aminoethyl)-1,5-dioxaspiro[5.5]undecane-2-acetic acid.

Aufarbeitung

temperatureThe suspension is cooled
filtrationfiltered
customto remove the Raney nickel
filtrationthrough filter aid
washthe precipitate is washed with methanol
concentrationThe filtrate is concentrated at reduced pressure
dissolutionThe residue is dissolved in methanol saturated with anhydrous ammonia
additiontreated with decolorizing charcoal
filtrationfiltered
filtrationthrough filter aid
customevaporated

Quellen und Nachweise

ORD-Eintrag: ord-7808c816b96844ee8740d34f9fc8f5f9
Quelldatensatz: uspto-grants-1991_03
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US05003080

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