HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533039Generated: October 29, 2026
Hydrochloric Acid → 3-(3,4-Dichlorophenyl)-4-(imidazol-1-yl)butan-1-ol
https://huagongshe.com/reaction/1533039
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(3,4-Dichlorophenyl)-4-(imidazol-1-yl)butan-1-al | HCID 22613804 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(3,4-Dichlorophenyl)-4-(imidazol-1-yl)butan-1-ol | HCID 22613829 | 85.5% |
Reaction Steps
Sodium borohydride (0.52 g) was added in three portions, over 5 minutes, to an ice-cooled solution of 3-(3,4-dichlorophenyl)-4-(imidazol-1-yl)butan-1-al (3.3 g) (see Preparation 18) in ethanol (25 ml). The mixture was stirred for a erther hour before removing the solvent under reduced pressure to give a residue. The residue was then suspended in water (50 ml), cooled to 0° C. and the mixture first acidified to pH1 with 2N aqueous hydrochloric acid solution and then basified to pH14 by addition of solid sodium carbonate before being extracted with ethyl acetate (3×200 ml). The organic phases were combined, dried over anhydrous sodium sulphate and the solvent removed under reduced pressure to yield 3-(3,4-dichlorophenyl)-4-(imidazol-1-yl)butan-1-ol (2.84 g) as a cream solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06207678B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-fc1082bbcbeb426abd734eeb633d146d |
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| Source note | uspto-grants-2001_03 |
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