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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 3-Methoxybenzaldehyde | HCID 11569 | — |
| Edukt | Cyclohexene, 1-((trimethylsilyl)oxy)- | HCID 81161 | — |
| Edukt | (R,R)-mono(2,6-dimethoxybenzoyl)tartaric acid | HCID 70267832 | — |
| Lösungsmittel | Propionitrile | HCID 7854 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (2R)-2-(1-hydroxy-1-(3-methoxyphenyl)methyl]cyclohexanone | HCID 70265867 | 149,5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06025375 |
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| Quelldatensatz | uspto-grants-2000_02 |
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| ORD ID | ord-2cf3118a80684934bb0069fd596a3ca9 |
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| Quellennotiz | uspto-grants-2000_02 |
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