HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → (4-Amino-3-bromophenyl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Acetylamino)-3-bromobenzeneacetic acid | HCID 20303412 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | (4-Amino-3-bromophenyl)acetic acid | HCID 20303490 | 91.4% |
Reaction Steps
30.5 g (0.112 mole) of 4-acetamido-3-bromophenylacetic acid are heated to 100° C. in 100 ml of 6 N hydrochloric acid until a clear solution forms, and the mixture is subsequently kept at 110° C. for one hour. Cooling is effected, followed by rendering alkaline with a solution of sodium hydroxide and acidifying with glacial acetic acid. The thus-formed flocculent precipitate is suction filtered, washed with water and dried to obtain 23.5 g (91.4% of theory) of 4-amino-3-bromophenylacetic acid (m.p. 139° to 140° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04239901 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-b757cdc7c78541d7b4e2ffb8d19bb4c8 |
| Source note | uspto-grants-1980_12 |