HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → N-(2-(thiophen-3-yl)ethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Thiophen-3-yl)ethan-1-amine hydrochloride | HCID 12258738 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-(thiophen-3-yl)ethyl)benzamide | HCID 25854160 | 96.1% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
2-(Thiophen-3-yl)ethanamine hydrochloride (3 g, 18 mmol) was taken in THF (40 mL) and treated with triethylamine (9.92 mL, 71.2 mmol). The reaction was cooled down to 0° C. and benzoyl chloride (2.55 mL, 21.9 mmol), diluted with THF was added dropwise to the reaction. The reaction was stirred for 3 h and the volatiles removed in vacuo. The residue was dissolved in ethyl acetate and washed with an aqueous saturated solution of sodium bicarbonate, water and brine. The organic solution was dried with sodium sulfate and purified by flash chromatography using a gradient of 25 to 70% ethyl acetate in hexanes to afford an off-white solid (4 g). MS (M+H)+ 232.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786132B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-75d55caffc664944a05ae28a9705c613 |
| Source note | uspto-grants-2010_08 |