HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891185Generated: October 30, 2026
Piconol → 9-((5-Hydroxypentyl)aminomethyl)anthracene
https://huagongshe.com/reaction/891185
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piconol | HCID 11474 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | HCID 22244783 | HCID 22244783 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 9-((5-Hydroxypentyl)aminomethyl)anthracene | HCID 10880907 | — |
Reaction Steps
The General Procedure for the N-Boc protection of N-(Anthracen-9-ylmethyl)amino alcohols 4 to give 5. The solution of N-(anthracen-9-ylmethyl)-amino alcohol (5 mmol) in 20 mL of pyridine-methanol (1:5 v/v) was stirred at 0° C. for 10 min. A solution of di-tert-butyl dicarbonate (7.5 mmol) in methanol (5 mL) was added dropwise over ten minutes. The temperature was allowed to rise to room temperature and the reaction was stirred overnight. The mixture was evaporated to dryness under reduced pressure. The residue was dissolved in methylene chloride, and washed with deionized water several times. The organic layer was separated, dried over anhydrous Na2SO4, filtered, and concentrated under vacuum. The residue was purified by flash chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001925B1 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-2f5380f1109a467c8233de729787448b |
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| Source note | uspto-grants-2006_02 |
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