HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850494Generated: October 31, 2026
Hydrochloric Acid → N-2-(4-hydroxyphenyl)ethyl-4-pentyloxyisoindoline
https://huagongshe.com/reaction/850494
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 19363249 | HCID 19363249 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-2-(4-hydroxyphenyl)ethyl-4-pentyloxyisoindoline | HCID 19363389 | 188.5% |
Reaction Steps
A suspension of LAH (40 mg, 1.1 mmol) in THF (1 ml) was added to a solution of N-2-(4-hydroxyphenyl)ethyl-4-pentyloxyphthalimide (208 mg, 0.59 mmol) in THF (1 ml) at 0° C. The mixture was stirred at room temperature for 3.5 hours. This reaction mixture was poured into a 3N aqueous hydrochloric acid solution (20 ml). The mixture was extracted with ethyl acetate (20 ml×3), and washed with a saturated aqueous sodium hydrogencarbonate solution (20 ml) and saturated brine (30 ml). The organic layer was dried over anhydrous magnesium sulfate. The drying agent was filtered of, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by column chromatography on silica gel (chloroform/methanol=30/1) to give N-2-(4-hydroxyphenyl)ethyl-4-pentyloxyisoindoline (181 mg, 94%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06017919 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-8a1b81e3178f4bf8b82f2dcc9edb29b6 |
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| Source note | uspto-grants-2000_01 |
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