HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 131720814, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Betulin | HCID 72326 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 131720814 | HCID 131720814 | 87% |
Reaction Steps
Then, the secondary hydroxyl group of monoprotected betulin compound 4 was acetylated using acetic anhydride in pyridine (Ac2O/pyridine), to yield monoprotected betulin acetate compound 5 of scheme 2 in 87% yield. Other acetylating agents also can be used. Examples of other acetylating agents include, but are not limited to, acetyl chloride; pentafluorophenyl acetate, triethylamine, and dimethylformamide; acetic anhydride, boron trifluoride etherate, and tetrahydrofuran; ketene, potassium tert-butoxide, and tetrahydrofuran; and acetic acid and trimethylsilyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05804575 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-aa279f192eda431db178ac2c07d6b0a9 |
| Source note | uspto-grants-1998_09 |