HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606643Generated: October 29, 2026
Dimethylformamide → HCID 67047531, compound
https://huagongshe.com/reaction/606643
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,4-Difluoro-3-methoxybenzoic acid | HCID 3780555 | — |
| Product | HCID 67047531 | HCID 67047531 | — |
Reaction Steps
To 10.0 g of 2,4-difluoro-3-methoxybenzoic acid was added 40 mL of tetrahydrofuran. To this solution was added 0.4 mL of N,N-dimethylformamide, and then 8 mL of thionyl chloride was added dropwise with stirring to this mixture at room temperature. After completion of the dropwise addition, Dimroth condenser was installed, and the mixture was heated under reflux for 2 hours. After allowing the reaction mixture to cool, the solvent was distilled away. The resulting acid chloride was dissolved in 40 mL of tetrahydrofuran, and 12 ml of triethylamine was added to this solution and the mixture was stirred. After 30 minutes, 8.37 g of ethyl N,N-dimethylaminoacrylate was added dropwise, and after completing the dropwise addition, the mixture was heated under reflux for 2 hours. After completion of the reaction, the precipitated solid was removed by suction filtration, and the filtrate was concentrated under reduced pressure to obtain 23.3 g of the desired title compound as a dark brown oily compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915418B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-de4f329d4faa4c968f6c8544368b45ec |
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| Source note | uspto-grants-2011_03 |
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