HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681130Generated: November 4, 2026
4-Methylbenzaldehyde → HCID 53981355, compound
https://huagongshe.com/reaction/1681130
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1,1,1-Trichloro-2,2,2-trifluoroethane | HCID 9635 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53981355 | HCID 53981355 | 390.7% |
Reaction Steps
12 g of p-tolualdehyde dissolved in 20 cc of DMF and 7.5 g of Zn are charged to a flask of 250 ml of capacity. 2.5 g of CF3CCl3 is dropwise added and the resulting reaction mixture is slightly heated until the reaction turns into strongly exothermic. Then 10 g of CF3CCl3 dissolved in 100 cc of DMF is dropwise added and the resulting mixture is stirred at room temperature for 4 hours. 10 cc of acetic anhydride and 13 g of Zn are then added. After 2 hours at room temperature, the reaction mixture is poured in acidic water and is extracted three times with ether; the ether phases are combined with one another, and are washed with a saturated solution of sodium bicarbonate, and with brine, and are then thoroughly dried and evaporated. The raw reaction product is chromatographed on silica (98/2 hexane/ethyl acetate). 11.5 g of 4-(2-chloro-3,3,3-trifluoroprop-1-enyl)-toluene is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05169848 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-a978f59029d24c7a8703d54b15d284c6 |
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| Source note | uspto-grants-1992_12 |
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