Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | (2s)-Cyclohexyl(hydroxy)acetic acid | HCID 819912 | — |
| Katalysator | Tetrabutylammonium Iodide | HCID 67553 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | Benzyl (s)-hexahydromandelate | HCID 54322505 | 77,5% |
Reaktionsschritte
A solution of 500 mg (3.2 mmol) of (S)-hexahydromandelic acid and 238 mg (0.6 mmol) of tetrabutylammonium iodide in 6.5 mL of CHCl3 was treated with 6.5 mL of 0.5 N KOH and 0.38 mL (3.2 mmol)of benzyl bromide then stirred at 70° C. for 1.5 h. The reaction was cooled to rt and the layers were separated. The aqueous phase was extracted with 2×50 mL CH2Cl2. The organic phases were combined, dried over Na2SO4 and concentrated. Flash chromatography using 17:3 v/v hexanes/EtOAc as the eluant afforded 616 mg (77%) of the title compound: RF: 0.37 (4:1 v/v hexanes/EtOAc); 1H NMR (300 MHz) δ 1.11-1.38 (m, 11H), 2.65 (d, J=6.3 Hz, 1H), 4.06 (dd, J=6.3, 3.5 Hz, 1H), 5.22 (s, 2H), 7.30-7.39 (m, 5H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06265434B1 |
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| Quelldatensatz | uspto-grants-2001_07 |
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| ORD ID | ord-69b560becb814bccb0784c184fa67963 |
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| Quellennotiz | uspto-grants-2001_07 |
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