HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623937Generated: October 29, 2026
Water → Tert-butyl 3-(5-bromopyrimidin-2-yl)oxy-2,2-dimethylpropanoate
https://huagongshe.com/reaction/623937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Bromo-2-chloropyridine | HCID 2734414 | — |
| Reactant | Tert-butyl 3-hydroxy-2,2-dimethylpropanoate | HCID 54272639 | — |
| Product | Tert-butyl 3-(5-bromopyrimidin-2-yl)oxy-2,2-dimethylpropanoate | HCID 67972905 | — |
Reaction Steps
In N,N-dimethylformamide (10 mL) were dissolved 5-bromo-2-chloropyridine (1000 mg) and tert-butyl 3-hydroxy-2,2-dimethylpropanoate (991 mg), and 60% sodium hydride (248 mg) was added to the solution under ice-cooling. The reaction mixture was stirred at room temperature for 6 hours, at 50° C. for 1 hour and 45 minutes, and then, at room temperature overnight. Water was added to the reaction mixture under ice-cooling, and the mixture was extracted with ether. The organic layer was separated, washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=100:0 to 95:5) to obtain tert-butyl 3-(5-bromopyrimidin-2-yl)oxy-2,2-dimethylpropanoate (1.048 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09302996B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-61eabace70ee45f9a9f7eb6bdf4c80ca |
|---|
| Source note | uspto-grants-2016_04 |
|---|