HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844556Generated: October 29, 2026
Hydrochloric Acid → 3-(3,4-Dichlorophenyl)-4-(imidazol-1-yl)butan-1-al
https://huagongshe.com/reaction/844556
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-(Imidazol-1-yl)-2-(3,4-dichlorophenyl)-3-(1,3-dioxolan-2-yl)propane | HCID 22613809 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(3,4-Dichlorophenyl)-4-(imidazol-1-yl)butan-1-al | HCID 22613804 | 46.2% |
Reaction Steps
5N Aqueous hydrochloric acid solution (100 ml) was added to an ice-cooled solution of 1-(imidazol-1-yl)-2-(3,4-dichlorophenyl)-3-(1,3-dioxolan-2-yl)propane (11 g) (see Preparation 17) in tetrahydrofuran (100 ml). The mixture was allowed to warm slowly to room temperature and then left to stand for 24 hours. The tetrahydrofuran was removed under reduced pressure and the acidic phase extracted with dichloromethane (2×100 ml). The organic phases were combined, washed with brine and dried over anhydrous sodium sulphate. The solvent was removed under reduced pressure to give the crude product which was chromatographed on silica gel eluting with a solvent gradient of 97.5:2.5 changing to 95:5, by volume, dichloromethane:methanol, to give 3-(3,4-dichlorophenyl)-4-(imidazol-1-yl)butan-1-al (4.4 g) as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06380396B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-12a464210ef44eb99546bc6281d3f9cb |
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| Source note | uspto-grants-2002_04 |
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