HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956163Generated: November 3, 2026
Dichloromethane → 5-Bromo-4-methoxypyrimidine
https://huagongshe.com/reaction/1956163
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 5-Bromo-4-chloropyrimidine | HCID 12270078 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-4-methoxypyrimidine | HCID 12270081 | — |
Reaction Steps
Twenty grams (0.13 mol) of 5-bromo-4-chloropyrimidine were dissolved in 100 mL of methanol and the solution was cooled to 5° C. by means of an ice bath. A solution consisting of 29.5 mL of a 25 percent solution of sodium methoxide in methanol and 20 mL of methanol was added with stirring and cooling. The temperature rose to 37° C. and then began to fall. The mixture was stirred for 4 hours at ambient temperature and was then diluted with 200 mL of water (which caused the formation of a white precipitate) and 200 mL of dichloromethane (which dissolved the precipitate). The phases were separated and the organic phase was washed with 150 mL of water, dried over sodium sulfate, and concentrated by evaporation under reduced pressure to obtain 18.2 g (93.8 percent of theory) of the title compound as a white crystalline solid melting at 73°-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05780465 |
|---|
| Source dataset | uspto-grants-1998_07 |
|---|
| ORD ID | ord-9db8ce25bb654458a9eb7d0b1ca34ce3 |
|---|
| Source note | uspto-grants-1998_07 |
|---|