HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20468635, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chloride | HCID 3017765 | — |
| Reactant | N-Methylaminoethanol | HCID 5247031 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20468635 | HCID 20468635 | 38.9% |
Reaction Steps
5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoyl chloride (7 g, 0.0184 mole) was added over 1 hr to a solution of N-methylaminoethanol (2.8 g, 0.0372 mole), triethylamine (3.7 g, 0.0368 mole) and THF (30 ml) at 25°-38°. The resulting mixture was heated to and held at reflux for 1.5 hrs., cooled and concentrated. The residue was taken into 400 ml of ether, washed three times with water, dried over MgSO4 and concentrated to 7.8 g of crude product. Kugelrohr distillation under reduced pressure afforded 3.0 g of pure N-(2-Hydroxyethyl)-N-methyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide as a gum; nmr (CDCl3) δ 2.95-3.08 (2S, 3H); 3.22-3.82 (m) 4.74 (s, 1H), 7.04-8.52 (m, 6H); ir (CHCl3) 3640, 3420, 1648 Cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04435588 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-286be7e07d8f48a9bba9c35cad4dcd67 |
| Source note | uspto-grants-1984_03 |