HuagongsheHuagongshe Chemistry Print Report · For research reference only
Catechol → Methyl 1,3-benzodioxole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl dichloroacetate | HCID 8315 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 1,3-benzodioxole-2-carboxylate | HCID 578017 | — |
Reaction Steps
Catechol (10.26 g, 93.2 mmol), sodium methoxide (25% by weight in methanol, 40.3 g, 186 mmol), and methyl dichloroacetate (13.3 g, 93.2 mmol) were combined in dry methanol (100 mL). The solution was heated to reflux overnight. The reaction was cooled to room temperature, acidified by addition of concentrated hydrochloric acid and then reduced in volume under vacuum to about 50 mL. Water was added and the mixture was extracted with diethyl ether (3×100 mL). The combined organic solution was dried with MgSO4, concentrated to a brown solid, and chromatographed (2% ethyl acetate in hexane) to yield benzo[1,3]dioxole-2-carboxylic acid methyl ester as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492431B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-3df122f0dab74b11bb90c3b973a37e48 |
| Source note | uspto-grants-2013_07 |