HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990273Generated: October 30, 2026
HCID 178442263, compound → Beta-Lapachone
https://huagongshe.com/reaction/990273
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178442263 | HCID 178442263 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Beta-Lapachone | HCID 3885 | — |
Reaction Steps
Into a 1,000 ml beaker containing sulfuric acid (300 ml), lapachol (30 g, 0.124 mol) was added in portions slowly over 5 minutes at room temperature while stirring vigorously. After addition, the dark mixture was stirred for an additional 30 min and then poured into ice water (800 g) with manual stirring in a 2,000 ml beaker. The mixture was transferred into a 2,000 ml separatory funnel and extracted twice with toluene (600 ml and 400 ml). The toluene phases were pooled and washed successively with 1% aqueous sodium chloride (800 ml), 1% aqueous sodium bicarbonate (400 ml) and 1% aqueous sodium chloride (800 ml), and then dried with sodium sulfate (50 g). After filtration, the filtrate was evaporated to dryness by Rotovap and then ethanol (300 ml) was added for co-evaporation to completely remove residual toluene. The residue was dissolved in 75% ethanol or absolute ethanol, preferably absolute ethanol (ethanol/water, 3:1, 300 ml) with heating in an 80° C. water bath, then was filtered and cooled to 4° C. slowly. Pure β-lapachone was isolated by filtration, then washed with cold 75% ethanol (4° C., 100 ml), dried under vacuum, packed under Argon atmosphere and stored at −20° C. in the dark.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458974B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-e0b516c9a5bb4144bcf52b3cc8afa580 |
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| Source note | uspto-grants-2002_10 |
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