HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483621Generated: October 28, 2026
2-Amino-2,3-dimethylbutanamide → HCID 15672411, compound
https://huagongshe.com/reaction/483621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Amino-2,3-dimethylbutanamide | HCID 9793773 | — |
| Reactant | HCID 15672403 | HCID 15672403 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15672411 | HCID 15672411 | 57.2% |
Reaction Steps
5-(1,3-Dioxepan-2-yl)-2,3-pyridinedicarboxylic acid, dimethyl ester (0.9 g, 0.00305 mol) in toluene is added to 2-amino-2,3-dimethylbutyramide (0.4 g, 0.00305 mol) and potassium tert-butoxide (0.69 g, 0.0061 mol) in toluene. The mixture is heated for 3 hours from 60° to 70° C. The reaction mixture is cooled to room temperature, water is added and the mixture is concentrated in vacuo to give an oil. The oil is diluted with water and washed with ether. The aqueous solution is acidified to pH 3.1 with 2 normal hydrochloric acid solution and extracted with methylene chloride. The combined methylene chloride extracts are dried over anhydrous magnesium sulfate and concentrated in vacuo to give the title compound as a white solid (0.63 g, 57%) mp 60°-69° C., identified by IR and NMR spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05225564 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-4cfd9707d72244ecaf17871baac8664f |
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| Source note | uspto-grants-1993_07 |
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