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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27699Erstellt: 26. Oktober 2026

Triethylamine → Cyano(6-phenoxy-2-pyridyl)methyl 2-(2-naphthyl)-3-methylbutanoate

https://huagongshe.com/reaction/27699

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktCyano(6-phenoxy-2-pyridyl)methanolHCID 12884337—
Edukt3-Methyl-2-(naphthalen-2-yl)butanoic acidHCID 13952228—
LösungsmittelDiethyl EtherHCID 3283—
ProduktCyano(6-phenoxy-2-pyridyl)methyl 2-(2-naphthyl)-3-methylbutanoateHCID 54346705—

Reaktionsschritte

To the acid chloride of 2-(2-naphthyl)-3-methylbutanoic acid (2.5 mmol) in ether is added 1.3 ml of triethylamine followed by the cyano(6-phenoxy-2-pyridyl)methanol in 5 ml of ether, from part A above, over about 2 minutes. The reaction mixture is stirred for about 18 hours and then quenched with saturated aqueous sodium bicarbonate. The organic phase is washed with aqueous sodium bicarbonate, water and brine, dried over calcium sulfate and solvent evaporated. The crude product is chromatographed on a circular chromatograph eluting with 20% ether/hexane to give cyano(6-phenoxy-2-pyridyl)methyl 2-(2-naphthyl)-3-methylbutanoate, MS m/e 436 (M+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04223033
Quelldatensatzuspto-grants-1980_09
ORD IDord-8dbca162771e40b0b5a7f74f9d9780a1
Quellennotizuspto-grants-1980_09