HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467060Generated: October 26, 2026
Water → 4-(4-Chlorophenyl)-1-(imidazol-1-yl)butan-2-one
https://huagongshe.com/reaction/467060
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-(4-chlorophenyl)-1-(1H-imidazol-1-yl)-2-butanol | HCID 10955994 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Chlorophenyl)-1-(imidazol-1-yl)butan-2-one | HCID 11010335 | 92.7% |
Reaction Steps
A solution of oxalyl chloride (74.8 g) in dry dichloromethane (1350 mL) at below -70° C. under a nitrogen atmosphere was treated with dry dimethyl sulfoxide (91.5 mL) in methylene chloride (270 mL) dropwise over 15 to 20 minutes while maintaining the temperature of the reaction mixture below -50° C. After an additional 5 minutes a solution of (±)-1-(4-(4-chlorophenyl)-2-hydroxybutyl)imidazole (128.3 g) in a mixture of dimethyl sulfoxide (50 mL) and methylene chloride (200 mL) was added over a period of 20 minutes keeping the reaction mixture at temperatures below -65° C. After a further 15 minutes dry triethylamine (300 mL) was added rapidly and after 15 minutes the reaction mixture was allowed to warm to 0° C. Water (20 mL) was then added to the reaction mixture, the methylene chloride then removed by evaporation and the resulting slurry was then treated with water and filtered. The filter cake was washed well with ice-water, cold ethyl acetate and then dried in air to yield 118.0 g of 4-(4-chlorophenyl)-1-(imidazol-1-yl)butan-2-one. The hydrochloride salt crystallized from methanol/acetone had a melting point of 172.5°-174.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05158949 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-f8e8e4a5050946c5a4b14e0ff1eaabc7 |
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| Source note | uspto-grants-1992_10 |
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