HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380113Generated: October 29, 2026
Potassium Hydroxide → HCID 20131160, compound
https://huagongshe.com/reaction/1380113
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Isopropyl 6-bromohexanoate | HCID 549816 | — |
| Reactant | HCID 13590265 | HCID 13590265 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 20131160 | HCID 20131160 | — |
Reaction Steps
1-[2-Hydroxy-3-[(4-methoxyphenyl)methoxy]propyl]-1H-imidazole (Example 1b; 10 g, 0.038 mol) was added to a stirred suspension of powdered potassium hydroxide (8 g, 0.14 mol) in dimethylsulphoxide (20 ml) at 18° C. and stirred for 0.5 hours. Isopropyl 6-bromohexanoate (10.5 g, 0.044 mol) was then added and the mixture was stirred for 0.5 hours at 18° C. The mixture was poured into saturated aqueous ammonium chloride (1500 ml) and extracted with dichloromethane. The combined extracts were dried (Na2SO4) and the solvent was evaporated off under reduced pressure to give the crude product which was purified by column chromatography (silica gel, 2% ethanol in chloroform) to give isopropyl 6-[2-(1H-imidazol-1-yl)-1-[[(4-methoxyphenyl)methoxy]methyl]ethoxy]hexanoate as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04579862 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-b73c89241d3841f9b687a95d2adf7234 |
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| Source note | uspto-grants-1986_04 |
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