HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1-Acetoxymethyl-4-chloro-3-(3,5-dichlorophenyl)pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undecen-7-ene | HCID 21979529 | — |
| Reactant | HCID 178478181 | HCID 178478181 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Acetoxymethyl-4-chloro-3-(3,5-dichlorophenyl)pyrazole | HCID 21852654 | — |
Reaction Steps
0.15 ml of 1,8-diazabicyclo(5.4.0)undecen-7-ene is added, at room temperature, to a solution of 2.55 g (0.01 mol) of 4-chloro-3-(3,5-dichlorophenyl)pyrazole and 0.90 g (0.030 mol) of paraformaldehyde in 70 ml of THF. The reaction mixture is stirred for 4 h at room temperature. A solution of 1.20 g (0.015 mol) of acetyl chloride in 10 ml of THF is run in dropwise at 0° C. and stirring is continued for 6 h at room temperature. The reaction mixture is concentrated to dryness. The residue is taken up in 15 ml of heptane and then dried. We obtain 3.05 g of 1-acetoxymethyl-4-chloro-3-(3,5-dichlorophenyl)pyrazole, melting at 95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05945382 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-f00980d8259a4f7ea58a2fcd92c6eba4 |
| Source note | uspto-grants-1999_08 |