HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404539Generated: October 25, 2026
Potassium Carbonate → Tert-butyl 2-cyano-2-(4,6-dimethoxypyrimidin-2-yl)acetate
https://huagongshe.com/reaction/404539
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl cyanoacetate | HCID 70693 | — |
| Reactant | 4,6-Dimethoxy-2-(methylsulfonyl)pyrimidine | HCID 838363 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 2-cyano-2-(4,6-dimethoxypyrimidin-2-yl)acetate | HCID 67959054 | — |
Reaction Steps
Into a 100-ml eggplant-shaped flask equipped with a magnetic stirrer and a reflux condenser were added 6.08 g (44 mmol) of potassium carbonate, 4.36 g (20 mmol) of 2-methanesulfonyl-4,6-dimethoxypyrimidine, 3.11 g (22 mmol) of tert-butyl cyanoacetate and 10 ml of N,N-dimethylformamide. The system inside was purged with nitrogen and stirred for 2 hours at 60° C. and for 4 hours at 70° C. The reaction slurry was cooled to room temperature and poured into 30 ml of a 5% aqueous hydrochloric acid solution. Thereto was added 50 ml of water, and concentrated hydrochloric acid was dropped until the system became acidic, followed by sufficient stirring. Then, filtration and washing with 30 ml of water were conducted. The crystals obtained were dried to obtain tert-butyl 2-cyano-2-(4,6-dimethoxypyrimidin-2-yl)acetate as white crystal of 5.4 g. HPLC purity: 99.3% Yield: 97%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748605B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-450ca218f0164befbe5ddaefb68b6ddf |
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| Source note | uspto-grants-2014_06 |
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