HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Baccatin Iii
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 10-deacetylbaccatin III | HCID 154272 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Catalyst | Scandium(III) triflate | HCID 2734571 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Baccatin Iii | HCID 65366 | 58% |
| Product | 10-deacetylbaccatin III | HCID 154272 | 18% |
Reaction Steps
To a solution of 50 mg (91.9 μmol) of 10-deacetylbaccatin III and 13 μL (1.5 eq.) of acetic anhydride in 2.0 mL of freshly distilled tetrahydrofuran 100 μL of a solution of 4.5 mg of commercial scandium trifluoromethanesulfonate in 1.0 mL of tetrahydrofuran was added. The reaction mixture was stirred at room temperature for 48 hours. Usual workup and isolation of the product by means of preparative TLC (Silica 60, CH2Cl2/MeOH 10:1) afforded 9 mg of unreacted 10-deacetylbaccatin III (18%) along with 31 mg of baccatin III (58%). 1H-NMR and Rf-value (TLC) were in accordance with the product from example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05874595 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-8d7679915d9c41e98caf514da8929edb |
| Source note | uspto-grants-1999_02 |