HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl 4-methoxyphenyl ketone → HCID 12795540, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Chloropyrimidin-2-ol hydrochloride | HCID 12648523 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12795540 | HCID 12795540 | — |
Reaction Steps
A suspension of 5-chloropyrimidin-2-one hydrochloride (502 mg), α-bromo-4-methoxyacetophenone (687 mg), triethylamine (1 ml) and ethanol (20 ml) was stirred at ambient temperature for 2 hours, during which the suspension formed a solution from which a solid crystallised out. The solid was crystallised from acetone to give the title pyrimidinone: yield. 449 mg; m.p. 212°-214° C.: λmaxEtOH 222.5 nm (ε 19850), 277 nm (ε 18000), 330 nm (ε 3725).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04636509 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-69281ac0830a4d729eb72f07ae8a88e6 |
| Source note | uspto-grants-1987_01 |