HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → (E)-N-[4-(chloromethyl)phenyl]3-(4-methylphenyl)cinnamamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | (E)-N-[4-(hydroxymethyl)phenyl]-3-(4-methylphenyl)cinnamamide | HCID 18472511 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (E)-N-[4-(chloromethyl)phenyl]3-(4-methylphenyl)cinnamamide | HCID 18472214 | — |
Reaction Steps
To a mixture of (E)-N-[4-(hydroxymethyl)phenyl]-3-(4-methylphenyl)cinnamamide (3.00 g), lithium chloride (741 mg), triethylamine (3.06 ml), DMAP(catalytic amount) and dichloro-methane (300 ml) was added methanesulfonyl chloride (1.15 ml), and the mixture was stirred at room temperature for 13 hours. To the reaction mixture was added 4N hydrochloric acid ethyl acetate solution (3.3 ml), and the mixture was purified with column chromatography (ethyl acetate) and recrystallized from ethyl acetatediisopropylether to give (E)-N-[4-(chloromethyl)phenyl]-3-(4-methylphenyl)cinnamamide (2.00 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166006 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-5c218cab46634052bf7c8d4f37cb8461 |
| Source note | uspto-grants-2000_12 |