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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 269425Erstellt: 27. Oktober 2026

Pyridine 4-methylbenzene-1-sulfonate → 7-Phenylhept-6-yn-1-ol

https://huagongshe.com/reaction/269425

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridine 4-methylbenzene-1-sulfonateHCID 161440—
Edukt2-(7-phenylhept-6-ynyloxy)tetrahydro-2H-pyraneHCID 58924678—
LösungsmittelMethanolHCID 887—
Produkt7-Phenylhept-6-yn-1-olHCID 5892467997%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

Pyridine toluene-4-sulphonate (0.75 g, 3 mmol) was added to a magnetically stirred solution of 2-(7-phenylhept-6-ynyloxy)-tetrahydro-2H-pyrane (7) (13.62 g, 50 mmol) in dry methanol (300 mL). The reaction mixture was stirred at 55° C. and monitored by TLC. When all the base material had been converted, methanol was distilled out on a rotary evaporator and water (200 mL) was added to the residue. The aqueous phase was extracted with petroleum ether (boiling point 40-60° C.)/Et2O 1:1 (5×50 mL). The combined organic phases were washed with water (2×20 mL) and dried (MgSO4). Distillation on a rotary evaporator yielded 9.1 g (97%) of a yellow viscous oil. TLC and NMR indicated a pure product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07446226B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-2facfffb0e2d44a9892ae3ed367c9f35
Quellennotizuspto-grants-2008_11