HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[3-(Chloromethyl)phenyl]methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 145883-50-7 | HCID 66630476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-(Chloromethyl)phenyl]methanesulfonamide | HCID 11053164 | — |
Reaction Steps
873 mg (4.903 mmol) of 3-(chloromethyl)aniline hydrochloride (Example 89A) were initially charged in 4 ml of tetrahydrofuran, and 2.48 g (24.514 mmol) of triethylamine were added. A solution of 421 mg (3.677 mmol) of methanesulfonyl chloride in 3 ml of tetrahydrofuran was slowly added dropwise, and the reaction solution was stirred at RT for 2 h. The reaction solution was concentrated using a rotary evaporator and the residue was purified by preparative HPLC (Chromasil, water/acetonitrile).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187428B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-95cd73e7c58a42cd92ad829c8a3f6e79 |
| Source note | uspto-grants-2015_11 |