HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409538Generated: October 31, 2026
Hydrochloric Acid → (2-chlorobenzyl)(4-chlorophenyl)methanone
https://huagongshe.com/reaction/1409538
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | 2-Chlorobenzyl chloride | HCID 11906 | — |
| Reactant | 4-Chlorobenzonitrile | HCID 12163 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Ether tetrahydrofuran | HCID 21868444 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2-chlorobenzyl)(4-chlorophenyl)methanone | HCID 246599 | 74% |
Reaction Steps
To diethylether (250 mL) was added magnesium (6.04 g) and a catalytic amount of iodine, and the mixture was stirred. Thereto was gradually added dropwise 2-chlorobenzyl chloride (20.0 g), and the mixture was stirred for 1 hour from the time when the temperature of such mixture began to rise. Thereto was added a solution of 4-chlorobenzonitrile (18.8 g) in tetrahydrofuran/diethylether (20 mL/50 mL), and the mixture was stirred for 3 hours. To the reaction mixture was added an aqueous 2N hydrochloric acid solution (150 mL) under ice-cooling, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed successively with water and brine, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo, and the resultant crude product was purified by column chromatography on silica gel (solvent: hexane/ethyl acetate=40/1 to 20/1) to obtain (2-chlorobenzyl)(4-chlorophenyl)methanone (24.40 g; yield: 74%) as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921380B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-9ab4f119dd754d1abf72537da05c7a8a |
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| Source note | uspto-grants-2014_12 |
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