HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13827107, compound → HCID 13827108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13827107 | HCID 13827107 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 13827108 | HCID 13827108 | — |
Reaction Steps
A solution of ethyl 2-ethoxycarbonylamino-4-nitro-6-ethyl-benzoate in tetrahydrofuran (10 ml) and sodium hydroxide (20 ml, 10%) was stirred at room temperature for 20 hours. The solution was extracted with ethyl acetate. The aqueous layer was acidified to pH=1 with 6M HCl, and then immediately extracted with ethylacetate. The ethyl acetate extract was washed with water and dried over magnesium sulphate. Solvent evaporation gave a solid which was further recrystallized from methylene chloride: petroleum ether to yield 2-ethoxycarbonylamino-4-nitro-6-ethyl benzoic acid, m.p. 121°-123° C. as orange crystals. IR νmax : 1665, 1720, 1620, 1510, 2500-3200(br), 3500cm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04873232 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-7662243cd25740088149a205f21452f2 |
| Source note | uspto-grants-1989_10 |