HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917374Generated: November 1, 2026
Dimethylformamide → HCID 69179367, compound
https://huagongshe.com/reaction/917374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Methyl-2-phenylpyrimidine-5-carboxylic acid | HCID 239975 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4,4-Difluoro-3-Methyl-3-Buten-1-Yl Methanesulfonate | HCID 23020237 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69179367 | HCID 69179367 | 73.3% |
Reaction Steps
To 5 ml of N,N-dimethylformamide were dissolved 0.34 g (1.6 mmol) of 4-methyl-2-phenylpyrimidine-5-carboxylic acid, synthesized in accordance with a method described in “J. Chem. Soc.”, page 2183 (1923), and 0.30 g (1.5 mmol) of 4,4-difluoro-3-methyl-3-butenyl methanesulfonate, followed by the addition of 0.27 g (3.2 mmol) of sodium hydrogencarbonate and stirring at 100° C. for 3 hours. The reaction liquid was then poured in water and extracted with diethtyl 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=1:4) to obtain 0.35 g (yield: 73%) of 4,4-difluoro-3-methyl-3-butenyl 4-methyl-2-phenylpyrimidine-5-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07273878B2 |
|---|
| Source dataset | uspto-grants-2007_09 |
|---|
| ORD ID | ord-d5834e2f2f6d421982344909185c0bdf |
|---|
| Source note | uspto-grants-2007_09 |
|---|