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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33718Erstellt: 23. Oktober 2026

Dichloromethane → Ammonia dichloromethane

https://huagongshe.com/de/reaction/33718

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktTriphenylphosphineHCID 11776—
Edukt1-Piperidinepropanol, 2-methyl-HCID 248806—
EduktDi-tert-butyl diazene-1,2-dicarboxylateHCID 6034084—
Edukt4-Piperidin-1-ylmethyl-phenolHCID 11636972—
Produkt2-Methyl-1-[3-(4-piperidin-1-ylmethyl-phenoxy)-propyl]-piperidineHCID 9945413—
ProduktAmmonia dichloromethaneHCID 227314292,5%

Reaktionsschritte

A suspension of the product of Example 17 (176 mg), 3-(2-methyl-piperidin-1-yl)-propan-1-ol (145 mg), and polymer supported triphenylphosphine (613 mg; loading: 3 mmol/g) in DCM (5 mL) was treated with di-tert-butylazodicarboxylate (316 mg). After 2 h, the resulting mixture was filtered, and the filtrate was evaporated. Chromatography of the residue (2.5% 2 M methanolic ammonia/DCM) gave the title compound as a colorless oil (60 mg). 1H NMR (400 MHz, CDCl3): 7.20 (d, J=8.6 Hz, 2H), 6.83 (d, J=8.6 Hz, 2H), 4.01-3.92 (m, 2H), 3.40 (s, 2H), 2.90-2.81 (m, 2H), 2.56-2.47 (m, 1H), 2.40-2.25 (m, 5H), 2.21-2.14 (m, 1H), 1.97-1.88 (m, 2H), 1.70-1.51 (m, 8H), 1.45-1.25 (m, 4H), 1.07 (d, J=6.2 Hz, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07429586B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-f4f114e9b4ef4aaebd94bc79e175298e
Quellennotizuspto-grants-2008_09