HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633719Generated: October 26, 2026
Ammonium Chloride → HCID 178526507, compound
https://huagongshe.com/reaction/1633719
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Iodo-1-tritylimidazole | HCID 618252 | — |
| Reactant | 5-Nitro-3,4-dihydronaphthalen-1(2H)-one | HCID 10261946 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178526507 | HCID 178526507 | — |
Reaction Steps
A solution of 4-iodo-1-trityl-1H-imidazole (5.5 g, 13 mmol) (prepared as described by Kirk, K. J. Heterocyclic Chem. (1985), 22, 57-59) in dichloromethane (50 mL) was treated with ethylmagnesium bromide (3.0 M in diethyl ether, 4.2 mL) over 4 minutes, stirred for 30 minutes, treated with 5-nitrotetralone (prepared as described by Zhang, M J. Amer. Chem. SoC, (1994), 116, 4852-4857), stirred for 6 hours, treated with ammonium chloride solution (50 mL) and extracted with a mixture of diethyl ether (300 mL) and ethyl acetate (50 mL). The organic layer was isolated, treated with dichloromethane (500 mL) to dissolve the product which started to crystallize, dried (MgSO4), filtered, concentrated, treated with trifluoroacetic acid (80 mL), stirred for 48 hours, concentrated to an oil, neutralized with sodium bicarbonate solution and extracted twice with dichloromethane. The combined dichloromethane layers were dried (MgSO4), filtered and concentrated. The residue was purified on silica gel with a gradient of 5%-10% methanol/dichloromethane to provide the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06503935B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-45768ce4f2fd4507887223018fed9d04 |
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| Source note | uspto-grants-2003_01 |
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