HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917372Generated: October 26, 2026
Dimethylformamide → HCID 69179458, compound
https://huagongshe.com/reaction/917372
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4,4-Difluoro-3-Methyl-3-Buten-1-Yl Methanesulfonate | HCID 23020237 | — |
| Reactant | 62724-87-2 | HCID 23272956 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69179458 | HCID 69179458 | 75.2% |
Reaction Steps
To 5 ml of N,N-dimethylformamide were dissolved 0.39 g (2.0 mmol) of 6-butoxynicotinic acid, synthesized by a method in accordance with one used in Intermediate Production Example 1, and 0.40 g (2.0 mmol) of 4,4-difluoro-3-methyl-3-butenyl methanesulfonate, followed by the addition of 0.34 g (4.0 mmol) of sodium hydrogencarbonate and stirring at 100° C. for 3 hours. The reaction liquid was then poured in water and extracted with diethyl ether. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentration under reduced pressure. The residue was purified with silica gel column chromatography (diisopropyl ether:hexane=1:7) to obtain 0.45 g (yield: 75%) of 4,4-difluoro-3-methyl-3-butenyl 6-butoxynicotinate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07273878B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-47d3cf1e3a0046b59dd9e976ab42940e |
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| Source note | uspto-grants-2007_09 |
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