HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → Ethyl 7-(Formylamino)chroman-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 7-Amino-2-chromancarboxylate | HCID 10632774 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 7-(Formylamino)chroman-2-carboxylate | HCID 20637412 | 100% |
Reaction Steps
Mixed anhydride is prepared by stirring 1.25 equivalents of formic acid and 1 equivalent of acetic anhydride at 60° C. for 2 h. A solution of ethyl 7-amino-2-chromancarboxylate (1.25 g; 5.6 mmol) in THF is treated with triethylamine (0.78 mL; 5.6 mmol) and the previously prepared mixed anhydride (1.6 mL), stirred at ambient temperature for 1 h, poured into a saturated aqueous solution of sodium bicarbonate and extracted with ethyl ether. The combined extracts are washed with brine, dried over MgSO4 and concentrated in vacuo to afford the title compound as a straw colored oil (1.4 g; 100%), identified by NMR spectral analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706757B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-8e07ca4e470c49a8820efd6faab7f6d4 |
| Source note | uspto-grants-2004_03 |