HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 23331358, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-(3-Methoxyphenyl)propan-2-amine | HCID 152234 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 23331358 | HCID 23331358 | — |
Reaction Steps
Methanesulfonyl chloride (131 g, 1.15 M) was added during 30 min to a solution of 2-(3-methoxyphenyl)-1-methylethylamine (189.7 g, 1.15 M) and triethylamine (116.7 g, 1.15 M) in benzene (2 l) with cooling to maintain an internal temperature of 20°-30°. The reaction was stirred at room temperature for 2 hr. The benzene solution was filtered from the triethylamine hydrochloride. The filter cake was washed with benzene (500 ml) and the combined filtrates were washed with 1 N. HCl (2×250 ml) and water (2×250 ml). The solution was dried over magnesium sulfate and then evaporated to give the sulfonamide as a thick oil. Wt=292 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04210749 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-dbf42ddeaf774f9bb3e69eaa01432aa5 |
| Source note | uspto-grants-1980_07 |