HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578620Generated: October 25, 2026
o-Phenetidine → N-(2-Ethoxyphenyl)-2-methylbenzamide
https://huagongshe.com/reaction/1578620
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | o-Phenetidine | HCID 7203 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | o-Methylbenzoyl bromide | HCID 2753161 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(2-Ethoxyphenyl)-2-methylbenzamide | HCID 576828 | 94.5% |
Reaction Steps
A 19.9 g (0.1 mol) portion of o-methylbenzoyl bromide was added dropwise with cooling to a mixture of 13.7 g (0.1 mol) of o-ethoxyaniline and 8.4 g (0.1 mol) of sodium bicarbonate in 200 ml of acetone with stirring. After addition of the o-methylbenzoyl bromide, the reaction mixture was warmed to 40°C and the mixture was refluxed and stirred for another 40 hours. After filtering, the ether was distilled from the reaction mixture and the residual material was re-dissolved in ether and washed with water. The ether layer was dried over anhydrous sodium sulfate, the ether was removed and the product was distilled to obtain 24.1 g (94.5%) of a clear pink liquid having a boiling point of 148°C/0.04 mm Hg and nD20 of 1.5929. IR cm-1 (film) νNH 3295(S), νCO 1655,1615(S).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03937840 |
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| Source dataset | uspto-grants-1976_02 |
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| ORD ID | ord-068254ea085449c08e495f0b93f9ea15 |
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| Source note | uspto-grants-1976_02 |
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