HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 69607348, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 69607391 | HCID 69607391 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69607348 | HCID 69607348 | — |
Reaction Steps
An ambient mixture of 2-(2-cyano-acetylamino)-4-(4-aminophenyl)-5-chloro-thiophene-3-carboxylic acid ethyl ester (365 mg, 1.00 mmol), NaHCO3 (210 mg, 2.50 mmol), and allyl bromide (0.173 mL, 2.00 mmol) in DMF (3.5 mL) was stirred for 18 h. The reaction was then diluted with H2O (5 mL) and Et2O (5 mL). The layers were separated, and the aqueous was extracted with additional Et2O (2×5 mL). The combined organic layers were dried with anhydrous Na2SO4, filtered, and concentrated under reduced pressure to an oil that was used without further purification. MS (ESI) m/e 442 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07119205B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-996e8eed09804ea99a7db888df3ca3d9 |
| Source note | uspto-grants-2006_10 |