HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521255Generated: October 30, 2026
HCID 57464094, compound → HCID 69507123, compound
https://huagongshe.com/reaction/521255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57464094 | HCID 57464094 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69507123 | HCID 69507123 | — |
Reaction Steps
To a stirred solution of 4-(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)butyraldehyde (8.0 g, 27.1 mmol) in anhydrous THF (270 mL) was added dropwise a solution of phenylmagnesium bromide (27.08 mL of a 1 M solution in THF). After 30 minutes, the solution was quenched with saturated ammonium chloride (100 mL), diluted with ethyl acetate (300 mL), and the layers separated. The organic solution was washed successively with a saturated aqueous sodium bicarbonate solution (100 mL) and brine (100 mL), dried over sodium sulfate, filtered, and concentrated to a light orange oil. Chromatography on silica gel (elution with 5% methanol in dichloromethane) provided 4-(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)-1-phenylbutan-1-ol (4.3 g) as a light orange, gummy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328110B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-68f6f53ac13c4c5880c576554077bf9d |
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| Source note | uspto-grants-2016_05 |
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