HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 4-chloro-2-(hydroxymethyl)-N-methylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 5-Chloro-1,3-dihydro-2-benzofuran-1-one | HCID 241737 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-chloro-2-(hydroxymethyl)-N-methylbenzamide | HCID 69180235 | — |
Reaction Steps
Methylamine gas was condensed into a sealed tube at −78° C., and a solution of 5-chloro-2-benzofuran-1(3H)-one (6.68 g, 39.8 mmol) in methanol (30 mL) was added. The solution was slowly warmed to room temperature overnight; The reaction was concentrated in vacuo, and the residue was partitioned between water and and chloroform. After three extractions with chloroform, the combined organics were dried over sodium sulfate, filtered, and concentrated in vacuo to afford 4-chloro-2-(hydroxymethyl)-N-methylbenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07323460B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-55e528e2c8444b6191108304948f3a54 |
| Source note | uspto-grants-2008_01 |