HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915982Generated: October 30, 2026
Dimethylformamide → HCID 136005822, compound
https://huagongshe.com/reaction/915982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 136005882 | HCID 136005882 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 136005822 | HCID 136005822 | 55.3% |
Reaction Steps
To a 3 ml tetrahydrofuran solution of 150 mg (0.36 mmol) of the compound obtained in Example 15, 0.45 ml of n-butyl lithium (1.59M hexane solution 0.72 mmol) was added dropwise at −78° C. After the mixture was stirred at the same temperature for 30 minutes, 33.4 μl (0.43 mmol) of N,N-dimethylformamide was added dropwise to the reaction mixture, followed by stirring the mixture at −78° C. for 2 hours. Then, an aqueous solution of ammonium chloride was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate, whereafter the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1) to obtain 73 mg (55%) of the captioned compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268128B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-c56d05d11a13459882d23983787af1a7 |
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| Source note | uspto-grants-2007_09 |
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