Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 71453801 | HCID 71453801 | — |
| Catalyst | Iron(3+) ethanedioate--water (2/3/6) | HCID 57370413 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 71455533 | HCID 71455533 | 42% |
Reaction Steps
A mixture of iron(III) oxalate hexahydrate (52.6 mg, 0.109 mmol, 30 equiv) in H2O was cooled to 0° C. and air was bubbled through the mixture for 10 minutes. A solution of 10′-chloroanhydrovinblastine (18a, 3.0 mg, 0.0036 mmol, 1 equiv) in H2O (0.5 mL), aqueous 0.1 N HCl (0.5 mL), and CF3CH2OH (0.1 mL) was transferred by pipette to the mixture and NaBH4 (2.7 mg, 0.073 mmol, 20 equiv) in H2O (1 mL) was added to the mixture at 0° C. The resulting mixture was stirred for 30 minutes before being quenched by addition of 28-30% aqueous NH4OH (10 mL). The mixture was extracted with 10% MeOH in CH2Cl2 and the organic layer was dried over Na2SO4 and concentrated under reduced pressure. PTLC (SiO2, Et3N:MeOH:EtOAc=3:3:97) provided 10′-chlorovinblastine (18b, 1.3 mg, 0.0015 mmol, 42%) as a white solid and 10′-chloroleurosidine (0.8 mg, 0.00095 mmol, 26%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940754B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-89e8745b45e64932ac63da7cafb28491 |
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| Source note | uspto-grants-2015_01 |
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