Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2226276Erstellt: 26. Oktober 2026

Hydrochloric Acid → Methyl 7-phenyl-3,5-dihydroxy-6-heptenoate

https://huagongshe.com/reaction/2226276

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktWaterHCID 962—
EduktSodium cyanoborohydrideHCID 5003444—
EduktMethyl 7-phenyl-5-hydroxy-3-oxo-6-heptenoateHCID 53740643—
KatalysatorChlorotitanium triisopropoxideHCID 3084342—
LösungsmittelMethanolHCID 887—
ProduktMethyl 7-phenyl-3,5-dihydroxy-6-heptenoateHCID 5438493465,2%

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

700 mg of methyl 7-phenyl-5-hydroxy-3-oxo-6-heptenoate (2.82 mmol) are dissolved in 25 cm3 of methanol and then cooled to -10° C. 0.71 cm3 of titanium chloride triisopropoxide (2.82 mmol) is added. The mixture is stirred for 20 minutes at -10° C. 207.8 mg of sodium cyanoborohydride (3.1 mmol) are then added and the mixture is then stirred for 3 hours 45 minutes at a temperature between -5° and 0° C. 5 cm3 of water and 1 cm3 of concentrated hydrochloric acid are added. After evaporation of the methanol under reduced pressure, the mixture is taken up in 50 cm3 of dichloromethane. The organic phase is washed with 25 cm3 of a saturated sodium bicarbonate solution and then with 25 cm3 of water and is then dried over sodium sulphate. After filtration and concentration to dryness, the residue obtained is treated with methanol. There is thus obtained, with a yield of 55%, 460 mg of methyl 7-phenyl-3,5-dihydroxy-6-heptenoate for which the syn/anti ratio is equal to 80/20.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05347039
Quelldatensatzuspto-grants-1994_09
ORD IDord-023e42b75a2240e9b7673525036c317b
Quellennotizuspto-grants-1994_09