HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonyl chloride | HCID 13424179 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonamide | HCID 13424180 | — |
Reaction Steps
A solution of 0.5 gram (0.002 mole) of 7-chlorosulfonyl-2,3-dihydro-2,2-dimethylbenzofuran and 4 ml of tetrahydrofuran was stirred and 2 ml of an aqueous solution of 29% ammonium hydroxide was added. The reaction mixture stirred for one hour, then was concentrated under reduced pressure to a residue. The residue was triturated with water and filtered to collect, when dried, 0.41 grams of 7-aminosulfonyl-2,3-dihydro-2,2-dimethylbenzofuran; m.p. 160.5°-162.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04743291 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-92e4df03ef304ea09130b8c314d3c4eb |
| Source note | uspto-grants-1988_05 |