HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 38202-27-6
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Mesitylenesulfonyl chloride | HCID 13046 | — |
| Reactant | Ethyl N-hydroxyacetimidate | HCID 5363167 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 38202-27-6 | HCID 6282444 | 64.5% |
Reaction Steps
To a solution of ethyl (1E)-N-hydroxyethanimidate (8.4 g, 81.5 mmol) in DMF (20 mL) is added triethylamine (12 mL, 86.24 mmol) and the mixture is stirred for 20 minutes. 2,4,6-Trimethylbenzene-1-sulfonyl chloride (20 g, 81.5 mmol) is added and the reaction mixture is stirred at room temperature for 16 hours. The reaction mixture is quenched with water (100 mL) and extracted with EtOAc (3×100 mL). The combined organic extracts are dried over sodium sulphate, filtered, and evaporated to dryness to give the title compound as white solid (15 g, 64%). The crude material is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120793B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-ac5865e2dcdc4a608ac1c14297bbddea |
| Source note | uspto-grants-2015_09 |