HuagongsheHuagongshe Chemistry Print Report · For research reference only
Catechol → 2,3-dihydro-1,4-benzodioxin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Catalyst | Trioctylmethylammonium chloride | HCID 21218 | — |
| Product | 2,3-dihydro-1,4-benzodioxin-2-one | HCID 4685450 | 61.3% |
Reaction Steps
To a stirred solution of 120 grams of catechol and 10 grams of Aliquat® 336 (brand of tricaprylmethylammonium chloride, of General Mills Chemical Company of Minneapolis, Minnesota) at 80° C. is added ethyl chloroacetate (87 grams, 1 mole) over a one hour period. The reaction mass is stirred for one hour and then cooled. 1000 ml of dilute (5%) hydrochloric acid is added with stirring. The aqueous layer is discarded. The organic layer is washed twice with a minimum amount of water. The toluene is distilled off under reduced pressure to afford 119 grams of crude product. Recrystallization from ethanol afforded 92 grams of 1,4-benzodioxan-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04294266 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-127b3ac12aa44f8da80407db6e53473a |
| Source note | uspto-grants-1981_10 |