Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 5-Chloro-2-ethoxybenzoyl chloride | HCID 12863234 | — |
| Reactant | Methyl 4-(2-aminoethyl)benzoate hydrochloride | HCID 13078671 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl Benzoate | HCID 7150 | — |
Reaction Steps
10.5 g of 4-(2-aminoethyl)-benzoic acid methyl ester-hydrochloride were suspended in 40 ml of dioxane and 20 ml of acetone and the suspension was combined with 8 ml of pyridine. To this suspension, a solution of 10 g of 2-ethoxy-5-chloro-benzoyl chloride in a small amount of acetone was added dropwise, while stirring, and the whole was heated for 2 hours under reflux. After cooling, the mixture was concentrated under reduced pressure, combined with ice-water, filtered with suction, stirred with dilute hydrochloric acid and with a NaHCO3 solution and the resulting product was again filtered off with suction and recrystallized from ethanol. The 4-(2-<2-ethoxy-5-chloro-benzamido>-ethyl)-benzoic acid methyl ester obtained was found to melt at 110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04221815 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-d8c8439507124513a02669ff6acf8f0e |
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| Source note | uspto-grants-1980_09 |
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