HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 12703974, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 12703694 | HCID 12703694 | — |
| Product | HCID 12703974 | HCID 12703974 | — |
Reaction Steps
Reaction of this 2-(4-methylphenyl)-4-methylpyrimidine with N-bromosuccinimide, as described in Example 15, affords 2-(4-bromomethylphenyl)-4-methylpyrimidine with a melting point of 104°-106° C. after recrystallisation from ligroin. A mixture of 105 g of 2-(4-bromomethylphenyl)-4-methylpyrimidine and 265 g of triethylphosphite is slowly heated, with stirring, to 150° C., while simultaneously distilling off ethyl bromide, and then stirred for 5 hours at this temperature. After distilling off excess triethylphosphite, the phosphate is obtained in a yield of 125 g in the form of a light brown viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04366189 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-3e75326c5bfe428d8dec091890146400 |
| Source note | uspto-grants-1982_12 |