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HRID 23713Erstellt: 24. Oktober 2026

Methylamine → tert-Butyl 2-oxo-2-(4-morpholin-4-ylphenyl)ethyl(methyl)carbamate

https://huagongshe.com/de/reaction/23713

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylamineHCID 6329—
Edukt2-Bromo-1-(4-morpholinophenyl)ethanoneHCID 2795357—
EduktCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-Butyl 2-oxo-2-(4-morpholin-4-ylphenyl)ethyl(methyl)carbamateHCID 2257434338%

Reaktionsschritte

2-Bromo-1-(4-morpholin-4-ylphenyl)ethanone (Tetrahedron Letters; 39, (1998), 4987-4990)(3.40 g, 11.97 mmol) was dissolved in dry THF (30 ml) under N2 and cooled in ice. A 2M solution of methylamine in THF (12 ml, 24 mmol) was added and the reaction stirred for 1 hr. The mixture was filtered and the filtrate treated with di-t-butyl carbonate (2.61 g, 12 mmol) at ice temperature. Stirring was continued for 24 hr then the solvent evaporated. Chromatography of the residue over silica gel (500 g) eluting with 1% MeOH-1% Et3N-EtOAc gave the product as a pale yellow solid (1.53 g, 38%): mp87-89°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852731B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-14a1a40fce874bbd8bc183963b270f71
Quellennotizuspto-grants-2005_02