HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 5-Ethoxycarbonylamino-2-(3,3,3-trifluoropropyl)-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Amino-2-(3,3,3-trifluoropropyl)benzofuran | HCID 22132957 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Ethoxycarbonylamino-2-(3,3,3-trifluoropropyl)-benzofuran | HCID 11130397 | 95.4% |
Reaction Steps
A solution of 2.0 g (8.7 mmol) of 5-amino-2-(3,3,3-trifluoropropyl) benzofuran in 30 ml of a 9/1 mixture of tetrahydrofuran and water is reacted for 30 min with 0.92 ml (9.6 mmol) of ethyl chloroformate in the presence of 1.1 g (13 mmol) of sodium hydrogen-carbonate. The reaction mixture is then diluted with water and dichloromethane, and then the organic phase is separated, dried over sodium sulfate and concentrated under reduced pressure. 2.5 g of product are obtained. Melting point: 108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06143772 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-3ca35e2895014cfba8cf76a6e1828cd2 |
| Source note | uspto-grants-2000_11 |