HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430769Generated: October 30, 2026
Tetrahydrofuran → HCID 18351660, compound
https://huagongshe.com/reaction/430769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 7-methoxy-1-benzofuran-3-carboxylic acid | HCID 12844603 | — |
| Reactant | 1-Hydroxy-4-phenylbutan-2-one | HCID 15090463 | — |
| Product | HCID 18351660 | HCID 18351660 | 47% |
Reaction Steps
7-methoxybenzofuran-3-carboxylic acid (220 mg) was dissolved in THF (5 ml). To this solution, 4-phenyl-2-oxo-1-butanol (211 mg) and dicyclohexylcarbodiimide (330 mg) were added and the resulting solution was stirred at room temperature for 16 hours. The reaction solution was filtered and the filtrate was poured into water layer (50 ml), followed by extraction twice with ethyl acetate (20 ml). The organic layers were combined and washed with saturated brine, followed by drying over sodium sulfate. After removing the sodium sulfate by filtration, the solvent was removed under reduced pressure and the residue was purified by column chromatography (solvent: hexane/ethyl acetate=3/1) using silica gel to obtain the desired compound (178 mg, yield: 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323235B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-3899f041d5c7434fa90e5f89861b1b1a |
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| Source note | uspto-grants-2001_11 |
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