Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20468635 | HCID 20468635 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20468617 | HCID 20468617 | 44.2% |
Reaction Steps
Acetyl chloride (2.7 g, 0.0344 mole) was added dropwise in 5 mins. to a solution of N-(2-hydroxyethyl)-N-methyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide (7.2 g, 0.0172 mole), triethylamine (25 ml) and THF (25 ml). The resulting mixture was heated up to and held at reflux for 2.5 hrs., cooled and concentrated. The residue was taken into 500 ml of ether, washed two times with water, dried over MgSO4 and concentrated to 8.6 g of crude product. The crude product was purified on a column of silica gel using ethyl acetate cyclohexane (1:3) as eluent to yield 3.5 g of pure N-[2-(acetoxy)ethyl]-N-methyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide as a gum; nmr (CDCl3) δ 2.04 (s, 3H), 2.92 (s)-3.15 (s) (3H), 3.40 (t)-3.79 (t) (2H); 4.12 (t)-4.40 (t) (2H), 6.80-8.42 (m, 6H); ir (CHCl3) 1750, 1655 Cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04435588 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-a0bce7b280ae4998a825408ded189c92 |
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| Source note | uspto-grants-1984_03 |
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