HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069200Generated: October 29, 2026
Dimethylamine → 2-benzyloxyimino-3-methoxyimino-N,N-dimethylbutyramide
https://huagongshe.com/reaction/1069200
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Benzyloxyimino-3-methoxyiminobutyric acid | HCID 54001678 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-benzyloxyimino-3-methoxyimino-N,N-dimethylbutyramide | HCID 54456661 | 53% |
Reaction Steps
To a solution of 0.9 g (3.6 mmol) of 2-benzyloxyimino-3-methoxyiminobutyric acid in 15 ml of toluene, 0.5 g (4.0 mmol) of thionyl chloride and one drop of N,N-dimethylformamide were added and the mixture was stirred for 1 hour at 60° C. After cooling with an ice, 5 ml of 50% dimethylamine solution was added and the mixture was stirred for 0.5 hour at room temperature. 30 ml of water was added and the mixture was extracted three times with 50 ml of diethylether. After washing with water and a saturated aqueous sodium chloride, the organic layer was dried over with anhydrous magnesium sulfate and the solvent was distilled off to obtain a residue, which was then purified by a column chromatography on a silica gel (n-hexane/ethyl acetate) to obtain 0.53 g (yield: 53%) of 2-benzyloxyimino-3-methoxyimino-N,N-dimethylbutyramide as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251949B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-abcb2cf2e4eb4c2494d9495d70b33a08 |
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| Source note | uspto-grants-2001_06 |
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