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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 377321Erstellt: 24. Oktober 2026

Hydrochloric Acid → (2R)-2-(1-hydroxy-1-(3-methoxyphenyl)methyl]cyclohexanone

https://huagongshe.com/reaction/377321

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt3-MethoxybenzaldehydeHCID 11569—
EduktCyclohexene, 1-((trimethylsilyl)oxy)-HCID 81161—
Edukt(R,R)-mono(2,6-dimethoxybenzoyl)tartaric acidHCID 70267832—
LösungsmittelPropionitrileHCID 7854—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(2R)-2-(1-hydroxy-1-(3-methoxyphenyl)methyl]cyclohexanoneHCID 70265867149,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of (R,R)-mono(2,6-dimethoxybenzoyl)tartaric acid (314 mg) in propionitrile (5 ml) was added 1M BH3 solution (1.0 ml) in tetrahydrofuran at 0° C. under N2. The reaction mixture was stirred for 1 hour at 0° C., and then the solution was cooled to -78° C. To this were added 1-(trimethylsilyl-oxy)cyclohexene (1.0 g) and 3-methoxybenzaldehyde (680 mg) successively. After stirring for 2 hours, the solution was poured into 1N-hydrochloric acid and the product was extracted with ether. The solvent was evaporated, and the residue was treated with 1N-hydrochloric acid-tetrahydrofuran solution (2 ml, 1:1). Usual chromatographic separation gave (2R)-2-(1-hydroxy-1-(3-methoxyphenyl)methyl]cyclohexanone (350 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06025375
Quelldatensatzuspto-grants-2000_02
ORD IDord-2cf3118a80684934bb0069fd596a3ca9
Quellennotizuspto-grants-2000_02