HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852247Generated: October 30, 2026
Diethylamine → N,N-diethyl-4-methoxy-2-methyl-benzamide
https://huagongshe.com/reaction/1852247
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | 4-Methoxy-2-methylbenzoic acid | HCID 597216 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | N,N-diethyl-4-methoxy-2-methyl-benzamide | HCID 11053218 | 57.6% |
Reaction Steps
4-methoxy-2-methylbenzoic acid (3.0 g, 18.05 mmol) was taken in thionyl chloride (20 ml) and refluxed for 1 h at 80° C. The reaction mixture was evaporated under reduced pressure. Under nitrogen the crude was quenched with diethyl amine (1.870 ml, 18.05 mmol) slowly under cooling conditions. The reaction mixture was dissolved in water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to get crude compound. The crude compound was purified by silica gel chromatography (20% ethyl acetate in pet ether) to get desired compound (2.3 g, 54.7%) as oil. 1H NMR (400 MHz, DMSO-d6): δ ppm 7.06-7.04 (d, J=8 Hz, 1H), 6.79 (s, 1H), 6.78-6.76 (d, J=8 Hz, 1H), 3.75 (s, 3H), 3.43 (br, s, 2H), 3.06-3.05 (m, 2H), 2.16 (s, 3H), 1.14 (d, J=8 Hz, 3H), 0.95 (d, J=8 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957203B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-0cadb5fb05b54698b318f40ed9189234 |
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| Source note | uspto-grants-2015_02 |
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