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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 372911Erstellt: 26. Oktober 2026

Water → Methyl 2-(3-benzyl-2-thienyl)-3-methoxypropenoate

https://huagongshe.com/reaction/372911

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTetrahydrofuranHCID 8028—
EduktMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
EduktHCID 14326170HCID 14326170—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDiethyl EtherHCID 3283—
ProduktMethyl 2-(3-benzyl-2-thienyl)-3-methoxypropenoateHCID 54504656—
ProduktHCID 67883648HCID 67883648—

Reaktionsschritte

Potassium tert-butoxide (844 mg) was added in one portion to a stirred suspension of (methoxymethyl)triphenylphosphonium chloride (2.86 g) in ether (30 ml). The reaction mixture became red. After 20 minutes, a solution of methyl 2-(3-phenoxymethyl-2-thienyl)-2-oxoacetate (770 mg) in THF (lOml) was added in one portion and the red colour was discharged. The resulting mixture was stirred at room temperature for 30 minutes then poured into water. The organic and aqueous layers were separated, and the latter was extracted with ether. The combined organic layers were washed with water, dried, concentrated and chromatographed using a 1:1 mixture of ether and petrol as eluent to give (i) the (Z)--isomer of the title compound (230 mg, 27%) as a pale yellow oil, lR (film) 1710, 1625 cm-1, 1H nmr : see Table VII; and (ii) the (E)-isom-er of the title compound (80 mg, 9% yleId), also a Pale yeIIow oil, IR (film) 1700, 1620 cm-1, 1H nmr : see Table VII.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05160364
Quelldatensatzuspto-grants-1992_11
ORD IDord-fb1f71a4d0814076a0161463b997299b
Quellennotizuspto-grants-1992_11