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HRID 2060744Erstellt: 25. Oktober 2026

Methylamine → (3,4-Dihydro-2H-pyran-2-ylmethyl)-methyl-amine

https://huagongshe.com/reaction/2060744

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylamineHCID 6329—
EduktAcrolein dimerHCID 60994—
EduktHCID 178418361HCID 178418361—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(3,4-Dihydro-2H-pyran-2-ylmethyl)-methyl-amineHCID 6013605185,1%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

3,4-Dihydro-2H-pyran-2-carbaldehyde (300 g, 2.68 mol) was dissolved in tetrahydrofuran (710 mL). Raney-Co catalyst (30 g, tetrahydrofuran moist) was added. Gaseous methyl amine (415.4 g, 13.4 mol) was transferred into the solution within 50 minutes (45° C.). Hydrogen (49.2 L) was added and the pressure adjusted to 100 bar and the solution was stirred for about 2 h at 100° C. The reaction vessel was cooled to room temperature, the gas removed and the solution degassed. The solution was concentrated under reduced pressure. The crude product (344.5 g) was distilled at reduced pressure to receive (3,4-Dihydro-2H-pyran-2-ylmethyl)-methyl-amine (289.8 g, 2.28 mol, 85% yield). Analytical data amine (3,4-Dihydro-2H-pyran-2-ylmethyl)-methyl-amine: Bp. 55-57° C. at 16 mbar; HPLC-MS: (M+H)+=128 at rt=0.619 min. (TIC), rt=0.596 min. (UV), rt=0.631 min. (ELS), Chromolith SpeedROD RP-18e 50-4.6 mm, solvent A: water+0.1% TFA, solvent B: acetonitrile+0.1% TFA, gradient: 4% solvent B at 0.0 min., 100% solvent B at 2.6 min., flow: 2.4 mL/min., UV: 220 nm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08278454B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-8b465595288a40ba984c52f2b05e8ace
Quellennotizuspto-grants-2012_10