HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → N-[4-(Bromoacetyl)phenyl]-N'-tert.-butylsulfamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | N-(4-acetylphenyl)-N'-tert.-butylsulfamide | HCID 21416935 | — |
| Catalyst | Bromine | HCID 24408 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[4-(Bromoacetyl)phenyl]-N'-tert.-butylsulfamide | HCID 21416979 | — |
Reaction Steps
A few drops of bromine (from a total of 10.3 g., 0.064 mole) is added to N-(4-acetylphenyl)-N'-tert.-butylsulfamide (17.3 g., 0.064 mole) in dioxane (200 ml.) solution at 15° C. and the solution is stirred until the color is discharged. The remainder of the bromine is added during 5 min. and the solution is stirred for an additional 10 min. thereafter. The solution is concentrated in vacuo and the residue triturated with isopropyl ether to give 20.7 g. (92%) of intermediate, recrystallized from isopropanol, m.p. 160.5°-161° C. (dec.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04044151 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-fcb7e3b91a394155a2661f7ee13a51b2 |
| Source note | uspto-grants-1977_08 |