HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508474Generated: October 28, 2026
Sodium Hydroxide → N'-[6-(3-tert-butyl-phenoxy)-5-methyl-pyridin-3-yl]-N-ethyl-N-methyl-formamidine
https://huagongshe.com/reaction/508474
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-ethyl-N-methylformamide | HCID 350667 | — |
| Reactant | 6-(3-Tert-butyl-phenoxy)-5-methyl-pyridin-3-ylamine | HCID 55080694 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N'-[6-(3-tert-butyl-phenoxy)-5-methyl-pyridin-3-yl]-N-ethyl-N-methyl-formamidine | HCID 25158780 | 86.5% |
Reaction Steps
In a 25 ml single-necked round-bottomed flask, ethylmethylformamide (350 mg) is solubilized in dry dichloromethane (4 ml) at ambient temperature (colourless solution). Under stirring phosphorous oxide chloride (0.4 ml) is added dropwise by syringe. Stirring at ambient temperature is continued for 0.5 hour, whereupon a pink-orange solution is obtained. To this solution, 6-(3-tert-butyl-phenoxy)-5-methyl-pyridin-3-ylamine (0.51 g) dissolved in 5.0 ml of dry dichloromethane is added dropwise by syringe, giving a yellow solution. Stirring is continued at an ambient temperature for 2 hours. The mixture is then poured into ice/water (pH=2, water phase). 2 M aqueous NaOH is then added to get a pH of about 11 and stirring is continued for 10 minutes. The mixture is then extracted with dichloromethane (2×50 ml). The combined organic phases are then dried over sodium sulfate, filtered and the solvent is removed in vacuo. Purification of this gum by flash chromatography over silica gel with ethyl acetate gives 0.56 g of the compound as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096525B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-8161fc170af84687963f5f496ded4ca9 |
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| Source note | uspto-grants-2015_08 |
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