HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 3-iodo-N,4-dimethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-Iodo-4-methylbenzoyl chloride | HCID 17752157 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-iodo-N,4-dimethylbenzamide | HCID 19688440 | 95% |
Reaction Steps
To a cooled (0° C.) solution of 3-iodo-4-methylbenzoyl chloride (2.80 g; 10.0 mmol) in DCM (10 mL) was slowly added a 2 M solution of methylamine in THF (11 mL, 2.2 eq.). Upon completion of the addition, the ice bath was removed and the mixture was stirred overnight. All volatiles were removed in vacuo and the residue was treated with aq. NaHCO3 (25 mL) and subsequently extracted with ethyl acetate (3×15 mL). The combined organic layers were dried over MgSO4 and evaporated. The target compound 3-iodo-N,4-dimethylbenzamide (2.62 g, 95% yield) was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642611B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-4d373b660c0a44c5833c706f21fb3554 |
| Source note | uspto-grants-2014_02 |