HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → (1-Trityl-1H-imidazol-4-YL)methyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | [1-(triphenylmethyl)-1H-imidazol-4-yl]methanol | HCID 382182 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (1-Trityl-1H-imidazol-4-YL)methyl acetate | HCID 10762461 | — |
Reaction Steps
Alcohol 2 (prepared above) was suspended in 500 mL of pyridine. Acetic anhydride (74 mL) was added dropwise, and the reaction was stirred for 48 hours during which it became homogeneous. The solution was poured into 2 L of EtOAc, washed with water (3×1 L), 5% aq. HCl soln. (2×1 L), sat. aq. NaHCO3, and brine, then dried (Na2SO4), filtered, and concentrated in vacuo to provide the crude product. The acetate 3 was isolated as a white powder (85.8 g) which was sufficiently pure for use in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06090948 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-42ff81219d564fc9af87512d5efd2219 |
| Source note | uspto-grants-2000_07 |