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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1780273Erstellt: 26. Oktober 2026

Tert-Butylamine → HCID 70051621, Verbindung

https://huagongshe.com/reaction/1780273

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-ButylamineHCID 6385—
EduktTriethylamineHCID 8471—
EduktP,P-Diphenylphosphinic azideHCID 199401—
Edukt(2S,4S)-1-((Benzyloxy)carbonyl)-4-hydroxypyrrolidine-2-carboxylic acidHCID 688414—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 70051621HCID 7005162124,7%

Reaktionsschritte

4.56 g (16.58 mmol) of diphenylphosphoryl azide, 1.50 g (20.55 mmol) of t-butylamine and 2.78 g (27.80 mmol) of triethylamine were successively added, whilst ice-cooling, to a solution of 3.68 g (13.90 mmol) of (4S)-1-benzyloxycarbonyl-4-hydroxy-L-proline in 30 ml of dimethylformamide, and the mixture was stirred for 5 hours. At the end of this time, the reaction mixture was poured into ice-water and extracted with ethyl acetate. The organic extract was washed with a 10% w/v aqueous solution of citric acid, with a 10% w/v aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, in that order, after which the resulting mixture was dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was recrystallized from a mixture of methylene chloride and diethyl ether, to give 1.10 g of the title compound as colorless crystals, melting at 129°-130° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05629406
Quelldatensatzuspto-grants-1997_05
ORD IDord-990d51f506bc475787cc715f1ac2efc1
Quellennotizuspto-grants-1997_05