HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-Nitro-5-(2,4,6-trichlorophenoxy)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-nitro-5-(2,4,6-trichlorophenoxy)benzoate | HCID 13013678 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Nitro-5-(2,4,6-trichlorophenoxy)benzoic acid | HCID 13013691 | 66.9% |
Reaction Steps
The product from paragraph (a) (6.86 g) in ethanol (50 ml) was heated and stirred with a solution of sodium hydroxide (0.8 g) in water (10 ml) at 60°-70° C. for 4 hours. The mixture was then cooled and the ethanol removed under reduced pressure. The residue was diluted to 100 ml with water and brought to pH 2 with concentrated hydrochloric acid. The solid which separated was collected and recrystallised from toluene to give the required benzoic acid derivative (4.26 g) with a melting point of 192°-192.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04285723 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-0285d12a4b87462aa2c6ac0498018813 |
| Source note | uspto-grants-1981_08 |