HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → n-Methyl-(2,5-dichlorothiophen-3-yl)carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2,5-Dichlorothiophene-3-carbonyl chloride | HCID 2777084 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | n-Methyl-(2,5-dichlorothiophen-3-yl)carboxamide | HCID 23434132 | 51% |
Reaction Steps
To a stirred solution of 2,5-dichloro-3-thenoyl chloride (commercially available from Maybridge Chemical Co. Ltd. 1.07 g, 5 mM) in CH2Cl2 (5 mL) was added 40% aqueous solution of methylamine (1 mL) at room temperature. After stirring overnight, the mixture was poured into CH2Cl2 (50 mL). The whole was washed with water (40 mL), brine (40 mL), dried over MgSO4, and concentrated in vacuo. The resulting solid was triturated with Et2O-hexane to give the subtitle compound (0.54 g, 51% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06048880 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-179a705b40474fd5a3f75b6658fc9395 |
| Source note | uspto-grants-2000_04 |