HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → ethyl 8-bromo-6-methoxy-4-oxo-4H-chromene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioic acid | HCID 69270394 | — |
| Product | ethyl 8-bromo-6-methoxy-4-oxo-4H-chromene-2-carboxylate | HCID 22142256 | 50% |
Reaction Steps
Sulfuric acid (50 ml) was added to (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioic acid (24.3 g, 86.6 mmol; as prepared in Reference Example 2b above). After heating the mixture with a heat gun for 5-10 min a clear deep brown solution was obtained. This solution was slowly added to refluxing absolute ethanol (250 ml). After the addition the reaction was refluxed for 30 min then allowed to cool. Crystals started to form after 20 min and the reaction was put in the refrigerator overnight. The solid was filtered, washed with cold ethanol/water 9:1 and dried to give ethyl 8-bromo-6-methoxy-4-oxo-4H-chromene-2-carboxylate as an off-white solid (12.3 g, 50% yield, mp 159-161° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07285662B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-64b368413a7d4ab48331f70a61faa0b2 |
| Source note | uspto-grants-2007_10 |