HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 176309-03-8
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-bromo-5-chlorosulfonyl-2-methyl-benzoic Acid | HCID 10757588 | — |
| Product | 176309-03-8 | HCID 22101346 | — |
Reaction Steps
74.1 g of 2-methyl-4-bromo-5-chlorosulphonylbenzoic acid [obtainable by reacting 2-methyl-4-bromobenzoic acid with chlorosulphonic acid] are stirred, at 10° and over a period of 1.5 h, into 170 ml of a 32% aqueous solution of ammonia, and this mixture is subsequently stirred at room temperature for 3 h. After that, the reaction mixture is concentrated, 50 ml of water are added, and this mixture is acidified with conc. HCl. The resulting precipitate is filtered off with suction and recrystallized from methanol. 2-Methyl-4-bromo-5-aminosulphonylbenzoic acid is obtained, m.p. 237°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849796 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-10e3bed155f74d98a30d146c505fe09f |
| Source note | uspto-grants-1998_12 |