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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4733Erstellt: 25. Oktober 2026

Hydrochloric Acid → z-Methyl-2-chloro-3-(4'-methoxyphenyl)propenoate

https://huagongshe.com/reaction/4733

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Eduktp-Methoxyphenyltrichlorovinyl carbinolHCID 15054139—
EduktSulfuric acid methanolHCID 18363649—
LösungsmittelWaterHCID 962—
Produktz-Methyl-2-chloro-3-(4'-methoxyphenyl)propenoateHCID 1233986599%

Reaktionsschritte

p-Methoxyphenyltrichlorovinyl carbinol (2.3 g, 8.6 millimoles) is added to a 40:60 (V/V) solution of sulfuric acid/methanol which is stirred under nitrogen at reflux (100° C.-106° C.) for 7 minutes. Rapid evolution of hydrogen chloride is noted and ceases after this period. The solution is cooled and poured into 40 ml of water, followed by extraction twice with 20 ml of methylene chloride each time. The organic phase is dried over MgSO4, filtered and rotary evaporated giving z-methyl-2-chloro-3-(4'-methoxyphenyl)propenoate (1.92 g, 8.5 millimoles) in 99 percent yield as a light yellow oil which crystallized on standing (M.P.=68° C.-70° C., M.P.LIT1 =67° C.-70° C.): 'H NMR (CDCl3) δ 7.24 (4H, ab quartet), 7.72 (1H, s), 3.76 (3H, s), 3.68 (3H, s); 13C NMR (CDCl3) δ 164.0, 161.1, 136.7, 132.6, 125.4, 119.0, 113.9, 55.2, 53.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04727181
Quelldatensatzuspto-grants-1988_02
ORD IDord-2a2734eb88c143a38c09acebdd4195a1
Quellennotizuspto-grants-1988_02