HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Benzyl-5-(bromomethyl)-3-(methylsulfanyl)benzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 20360840 | HCID 20360840 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Benzyl-5-(bromomethyl)-3-(methylsulfanyl)benzene-1-sulfonamide | HCID 20294546 | — |
Reaction Steps
4-Benzyl-3-methylthio-5-sulfamylbenzyl alcohol (10 g; prepared as described in Example 1) is while stirring added in portions to acetic acid saturated with dry hydrogen bromide (50 ml), and the mixture is stirred for 24 hours. The resulting solution is diluted with water (100 ml) and cooled to precipitate crude 4-benzyl-3-methylthio-5-sulfamylbenzyl bromide. After recrystallization from methanol it is obtained with a melting point of 149°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04082851 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-ef3cca4b265c4bd985f8e350a76d95c7 |
| Source note | uspto-grants-1978_04 |