HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → N-methyl-4-(4-chlorophenoxy)benzene-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-(4-Chlorophenoxy)benzene-1-sulfonyl chloride | HCID 2757750 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-methyl-4-(4-chlorophenoxy)benzene-sulfonamide | HCID 18549775 | — |
Reaction Steps
To 20 ml of a 2 molar solution of methylamine in tetrahydrofuran chilled in an ice bath was added a solution of 5.16 g of 4-(4-chlorophenyloxy)benzene-sulfonyl chloride in 50 ml of tetrahydrofuran and 20 ml of CH2Cl2. The mixture was refluxed for 2 hours and the solvent removed under vacuum and the residue partitioned between CH2Cl2·H2O (1:1). The CH2Cl2 layer was separated and washed with 2 N citric acid, brine and dried (Na2SO4). The solution was filtered through a thin pad of hydrous magnesium silicate and the filter pad washed with CH2Cl2. The filtrate was concentrated to give 4.5 g of N-methyl-4-(4-chlorophenoxy)benzene-sulfonamide as a yellow solid, m.p. 80-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498167B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-2fb4db9ea22343bd886d76dac59f9c62 |
| Source note | uspto-grants-2002_12 |