HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608787Generated: October 30, 2026
N-Methylaniline → Butanoic acid, 4-(methylphenylamino)-
https://huagongshe.com/reaction/1608787
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methylaniline | HCID 7515 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Butanoic acid, 4-(methylphenylamino)- | HCID 11160218 | 84% |
Reaction Steps
A mixture of N-methylaniline (10 g), ethyl 4-bromobutyrate (13.2 ml) and potassium carbonate (12.7 g) was stirred for 1.5 hour at 110° C. After cooling to room temperature, ethanol (100 ml) and 3N aqueous sodium hydroxide (100 ml) were added to the mixture, and the mixture was stirred for 30 minutes under reflux. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure and the residue was diluted with water and then washed with ether. The aqueous layer was acidified to pH 4 with concentrated hydrochloric acid and extracted three times with ethyl acetate. The organic layers were collected and extracted twice with 3N hydrochloric acid. The aqueous layers were collected, adjusted to pH 4 by using 20% NaCl aqueous solution, and extracted five times with an ethyl acetate. The combined organic layer was washed with water and saturated sodium chloride, dried over anhydrous sodium sulfate and then concentrated under reduced pressure to give 14.8 g (84%) of the objective compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05397781 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-8667cb695c85482298fa2fa2149fb5ad |
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| Source note | uspto-grants-1995_03 |
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