HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903560Generated: October 30, 2026
2,3-Dichlorobenzoyl chloride → HCID 20242181, compound
https://huagongshe.com/reaction/1903560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichlorobenzoyl chloride | HCID 17944 | — |
| Reactant | HCID 178418822 | HCID 178418822 | — |
| Reactant | HCID 178477959 | HCID 178477959 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20242181 | HCID 20242181 | — |
Reaction Steps
2.88 g of 4-phenylimidazole are dissolved in 7 ml of tetrahydrofuran; a solution of 2.12 g of dichlorobenzoyl chloride in 5 ml of tetrahydrofuran is then added, and the mixture is heated, in the course of which 4-phenylimidazole hydrochloride precipitates. The mixture is diluted with 15 ml of tetrahydrofuran, and is filtered at room temperature in vacuo. The filtrate is subsequently evaporated to dryness in a rotary evaporator, and the residue is recrystallised from 15 ml of ethyl acetate. The yield is 1.55 g (48.9% of theory) of the desired product, m.p. 135°-136° C. By concentration of the mother liquor by evaporation and recrystallisation from 8 ml of benzene, there are obtained a further two fractions (0.76 g, m.p. 135°-136° C.; and 0.41 g, m.p. 134°-135° C.). The total yield is hence 2.72 g (85.8% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04436892 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-0cb65022f236453cbf8d1e2f1ba20e69 |
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| Source note | uspto-grants-1984_03 |
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