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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 536580Erstellt: 26. Oktober 2026

Tert-Butylamine → Tert-butyl 5-formyl-6-azaspiro[2.5]octane-6-carboxylate

https://huagongshe.com/reaction/536580

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-ButylamineHCID 6385—
Edukt(S)-2-[tert-butoxycarbonyl-(2-methoxycarbonyl-ethyl)-amino]-succinic acid 4-methyl esterHCID 10936520—
EduktSodium methanolate methanolHCID 23694274—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 5-formyl-6-azaspiro[2.5]octane-6-carboxylateHCID 8666486555,7%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

To a solution of (S)-2-[tert-Butoxycarbonyl-(2-methoxycarbonyl-ethyl)-amino]-succinic acid 4-methyl ester (intermediate 12, 420 g, 1.35 mol) in THF (2 L) under nitrogen cooled to 0° C. was added NaOMe/MeOH (1.5 L, 2.7M) in half an hour. The resulting yellow solution was stirred at 85° C. for 3 hours (after 1 hour a suspension was obtained). THF (1.5 L) was distilled off under the reduced pressure and water (2 L) was added. The resulting mixture was stirred at 110° C. for 20 hours. The mixture was washed with ethyl acetate (2×1 L). The aqueous solution was cooled to 0° C. and the value of pH was adjusted to 2.5 with concentrated HCl. The product was extracted with ethyl acetate (3×1 L) and the organic extracts were combined, washed with saturated NaCl (1 L), dried (Na2SO4) and filtered. The filtrate was cooled to 0° C. and tert-butylamine (145 ml, 1.35 mol) was added with stirring. The yellow solid was collected by filtration and dried, then boiled in isopropyl alcohol (1.5 L). The suspension was cooled to 5° C. and collected by filtration to give 180 g of intermediate 3 (light white solid, yield:45%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859608B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-2f4ec597ed5948fe8457c8b86be28fb3
Quellennotizuspto-grants-2014_10