HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012460Generated: October 27, 2026
Iodine → Ethanone, 2-chloro-2,2-difluoro-1-(2-methylphenyl)-
https://huagongshe.com/reaction/1012460
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | 2-Bromotoluene | HCID 7236 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Chlorodifluoroacetic acid | HCID 66154 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethanone, 2-chloro-2,2-difluoro-1-(2-methylphenyl)- | HCID 66974611 | 31.2% |
Reaction Steps
Magnesium (flake, 6.2 g) was suspended in diethyl ether (10 mL), and iodine (small amount) was added and a solution of 2-bromotoluene (43.26 g) in diethyl ether (100 mL) were slowly added dropwise. After stirring at room temperature for 1 hr, the reaction mixture was added dropwise to a solution of chlorodifluoroacetic acid (10.0 g) in diethyl ether (100 mL) at −10° C., and the mixture was stirred at 0° C. for 1 hr. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with diethyl ether. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was distilled under reduced pressure (boiling point: 81-82° C./12-13 mmHg) to give the title compound as a pale-yellow oil (yield 4.9 g, 31%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977488B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-b89ff84d12f5437f9dee87f1654ce523 |
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| Source note | uspto-grants-2011_07 |
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