HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → o-Chlorophenylacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86739887 | HCID 86739887 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Water | HCID 962 | — |
| Product | o-Chlorophenylacetic acid | HCID 17124 | 95% |
Reaction Steps
225.5 g (1 mol) of N-t.-butyl-(2-chlorophenyl)-acetamide (melting point: 128°-130° C.) and 281 g of 15% strength NaOH (1.05 mols) are heated at 260° C., while stirring, for 3 hours in a 0.7 l nickel autoclave. The autoclave is cooled and the reaction mixture is run into a distillation apparatus. Distillation through a 30 cm column up to a head temperature of 100° C. gives 71.5 g of t.-butylamine of 97% purity, corresponding to a yield of 95% of the theoretical yield. 200 ml of water and 100 ml of 30% strength hydrochloric acid are added to the distillation bottom product. The acid which has been precipitated is filtered off with suction and dried in vacuo. 157.8 g of o-chlorophenylacetic acid of melting point 95° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04496736 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-a0d7333184654f28a7876d6f32d9a2f7 |
| Source note | uspto-grants-1985_01 |