HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22178Generated: October 28, 2026
Hydrochloric Acid → 6-ethyl-N,N-dimethyl-2-methoxy-benzamide
https://huagongshe.com/reaction/22178
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 2-Methoxy-N,N-dimethylbenzamide | HCID 11159646 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Cyclohexane isopentane | HCID 19019564 | — |
| Product | 6-ethyl-N,N-dimethyl-2-methoxy-benzamide | HCID 19927392 | — |
Reaction Steps
39.5 g of N,N-dimethyl-2-methoxy-benzamide and 28.5 ml of tetramethylethylenediamine are introduced into 190 ml of absolute tetrahydrofuran and the mixture is lithiated at -70° C. with 150 ml of a 1.4-molar sec-butyllithium solution in cyclohexane/isopentane. After subsequently stirring at -70° C. for 45 minutes, 25.6 ml of ethyl bromide are added dropwise within 25 minutes and the reaction mixture is then allowed to warm slowly to room temperature. Water is then added and the mixture is adjusted to pH 2 with hydrochloric acid and extracted twice with diethyl ether. The residue is purified on silica gel using ethyl acetate/n-hexane (4:6) to yield 6-ethyl-N,N-dimethyl-2-methoxy-benzamide in the form of a colourless oil, 1H-NMR (CDCl3): 3.82 ppm (m), 3.40 ppm (m) and 3.12 ppm (2q, N(CH2CH3)2), 2.56 ppm (m, CH2CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05428002 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-e236a500874a40a585bf4dcbacb3eccc |
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| Source note | uspto-grants-1995_06 |
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