HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-[3-(4-Chlorophenyl)-1,2-oxazol-5-yl]methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 4-Chloro-benzaldehyde oxime | HCID 219158 | — |
| Reactant | Propargylamine | HCID 239041 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[3-(4-Chlorophenyl)-1,2-oxazol-5-yl]methanamine | HCID 2764163 | 110.2% |
Reaction Steps
1.56 g (10 mmol) of p-chlorobenzaldoxime was dissolved in 40 ml of dried dichloromethane in a erlenmeyer flask equipped with a magnetic stirrer, and 1.7 g (12 mmol) of N-chlorosuccinimide was added slowly. The reaction mixture was stirred until completely dissolved. The system was heated slightly for 20 min. Then, 0.56 g (10 mmol) of propargyl amine was introduced and 1.2 g (12 mmol) of triethylamine was added dropwise, which caused the emission of white smog. The reaction mixture was heated under reflux for 2 h, and then purified by column chromatography on silica gel using petroleum ether (b.p. 60-90° C.)—ethyl acetate (v:v=4:1) as eluant, to obtain 2.3 g of the product as yellow solid. The yield was 62%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790759B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-e229fd65466c4afa88552f7c6d1dd472 |
| Source note | uspto-grants-2010_09 |