HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 12703975, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 12703695 | HCID 12703695 | — |
| Product | HCID 12703975 | HCID 12703975 | — |
Reaction Steps
Reaction of the above 2-(4-methylphenyl)-5-methylpyrimidine with N-bromosuccinimide, as described in Example 15, affords 2-(4-bromomethylphenyl)-5-methylpyrimidine with a melting point of 129°-131° C. (recrystallisation from ligroin). With stirring, a mixture of 184 g of 2-(4-bromomethylphenyl)-5-methylpyrimidine and 465 g of triethylphosphite is slowly heated to 150° C., while simultaneously distilling off ethyl bromide, and then stirred for 5 hours at this temperature. Excess triethylphosphite is distilled off, affording 220 g of the phosphonate 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-20d5360304c947f9a1686b2ce3153512 |
| Source note | uspto-grants-1982_12 |