HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857733Generated: October 31, 2026
Ammonium Chloride → [2-benzyloxymethyl-5-isopropyl-3-methyl-3H-imidazol-4-yl]-(3,5-dichlorophenyl)-methanol
https://huagongshe.com/reaction/1857733
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3,5-Dichlorobenzaldehyde | HCID 35746 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | 2-((benzyloxy)methyl)-4-iodo-5-isopropyl-1H-imidazole | HCID 178440140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-benzyloxymethyl-5-isopropyl-3-methyl-3H-imidazol-4-yl]-(3,5-dichlorophenyl)-methanol | HCID 22130494 | 33.4% |
Reaction Steps
In 30 ml of dry tetrahydrofuran was dissolved 3.31 g (8.94 mmol) of 2-benzyloxymethyl-5-iodo-4-isopropyl-1-methylimidazole (4c), followed by addition of 5.78 ml (9.83 mmol) of n-butyllithium (1.70 M hexane solution) at -70° C. over 30 minutes. Then, after 5 minutes, a solution of 1.56 g (8.91 g) of 3,5-dichlorobenzaldehyde dissoloved in 10 ml of dry tetrahydrofuran was added at -70° C. over 30 minutes. After 1 hour, the mixture was left to cool to room temperature, and an aqueous solution of ammonium chloride was added thereto, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel chromatography (ethyl acetate/methylene chloride 10:1) to give 1.25 g of [2-benzyloxymethyl-5-isopropyl-3-methyl-3H-imidazol-4-yl]-(3,5-dichlorophenyl)-methanol (56) (yield 33.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06147097 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-f9b91a8c7888492fbd96ebdcbf6623d0 |
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| Source note | uspto-grants-2000_11 |
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