HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Acetoxymethylindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1H-indol-4-ylmethanol | HCID 2773457 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Acetoxymethylindole | HCID 20132383 | — |
Reaction Steps
4-Hydroxymethylindole (17 g) is heated in pyridine (12 ml) with acetic anhydride (11.9 ml) for three hours on the steam bath. After dilution with ether, the reaction mixture is first shaken out with 1N hydrochloric acid, then with saturated sodium bicarbonate solution and finally with water. The ether solution is evaporated. 20 g of 4-acetoxymethylindole remains.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04731365 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-f5a6e312d5b741aaa43bf70079b5d383 |
| Source note | uspto-grants-1988_03 |