HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26243Generated: October 29, 2026
Hydrochloric Acid → 1-[3-(Trifluoromethoxy)phenyl]propan-2-one
https://huagongshe.com/reaction/26243
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-(3'-Trifluoromethoxyphenyl)-2-nitro-propene | HCID 53911105 | — |
| Catalyst | Iron | HCID 23925 | — |
| Product | 1-[3-(Trifluoromethoxy)phenyl]propan-2-one | HCID 21325271 | 55% |
Reaction Steps
29 g (117 mmols) of 1-(3'-trifluoromethoxy-phenyl)-2-nitro-propene, 46 g (0.82 g atom) of iron powder, 0.6 g of ferric chloride and 120 ml of water are introduced into a 500 ml three-necked flask equipped with a mechanical stirrer, a condenser and a dropping funnel, and this mixture is heated at 80° C. 29 ml of concentrated hydrochloric acid are added dropwise, via the dropping funnel, with stirring, over the course of 5 hours, while the temperature is kept at 80° C. The reaction mixture is allowed to cool overnight. The ketone is then steam distilled. The distillate is extracted twice in succession with 100 ml of diethyl ether each time. The two ether extracts are combined, dried over sodium sulphate and filtered. The solvent is evaporated from the filtrate in vacuo on a water bath, and the residue is rectified. 14,15 g (55% yield) of 1-(3'-trifluoromethoxy-phenyl)-2-propanone are thus obtained as a liquid, b.p. 112°- 118° C./18 mm.Hg, nD21°5 =1.448.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04148923 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-8c9b93c0c5ea4767bdd610ba686675cd |
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| Source note | uspto-grants-1979_04 |
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