HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 54254236, compound → 2-Chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4-trifluoromethyl-1(2H)-pyrimidinyl]benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 54254236 | HCID 54254236 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4-trifluoromethyl-1(2H)-pyrimidinyl]benzaldehyde | HCID 21201225 | — |
Reaction Steps
A solution of 20.08 g of 2-chloro-5-[3,6-dihydro-2,6-dioxo-3-methyl-4-trifluoromethyl-1(2H)-pyrimidinyl] benzyl alcohol in 250 ml dichloromethane is added dropwise in the course of 30 minutes with stirring at room temperature to a suspension of 19.38 g of pyridinium chlorochromate in 250 ml of dichloromethane, and stirring of the reaction mixture is continued for 3 hours at 25°-28° C. The clear solution is decanted, the brown residue is washed with 100 ml of dichloromethane, and the dichloromethane solution is filtered through 150 g of silica gel. The filtrate is concentrated, and the residue is recrystallised from n-hexane/ethyl acetate; m.p.: 168°-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05336663 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-e774e53f348f48738a5e63ca84583c34 |
| Source note | uspto-grants-1994_08 |