Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 3-Methoxybenzenesulfonyl chloride | HCID 2737504 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10752756 | HCID 10752756 | 92.6% |
Reaction Steps
49.5 gm (0.24 mol) of 3-methoxy-benzene sulfonic acid chloride were dissolved in 50 ml of tetrahydrofuran, and the solution was added dropwise over a period of 25 minutes to a solution of 40 gm (0.55 mol) of tert. butylamine in 200 ml of tetrahydrofuran. After stirring for 1 hour at room temperature and for 7 hours at 60° C., the reaction mixture was filtered, and the filtrate was evaporated in vacuo. The residue was treated with cyclohexane, yielded 54.1 gm (92.6% of theory) of N-tert. butyl-3-methoxy-benzenesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04404230 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-8ecaac07fa044b289f88f0611c5debf1 |
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| Source note | uspto-grants-1983_09 |
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