HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234255Generated: October 25, 2026
Water → (Z)-5-Acetylamino-2,4,6,7-tetramethyl-2-styryl-2,3-dihydrobenzofuran
https://huagongshe.com/reaction/234255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 19078578 | HCID 19078578 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Catalyst | Benzyltriphenylphosphonium chloride | HCID 70671 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Z)-5-Acetylamino-2,4,6,7-tetramethyl-2-styryl-2,3-dihydrobenzofuran | HCID 67671450 | 77.2% |
Reaction Steps
A suspension of benzyltriphenylphosphonium chloride (0.7 g, 1.8 mmol) in tetrahydrofuran (10 ml) was cooled to -20° C. and n-butyllithium hexane solution (1.6M, 1.12 ml, 1.8 mmol) was added dropwise. The reaction mixture was stirred for 30 minutes and then a solution of 5-acetylamino-2-formyl-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran (0.45 g, 1.7 mmol) in tetrahydrofuran (5 ml) was added. The reaction mixture was stirred at room temperature for additional 30 minutes. Water was added to the reaction mixture and the product was extracted with ethyl acetate. The extract was washed with water, dried and then concentrated. The residue was purified by column chromatography on silica gel (isopropyl ether-ethyl acetate, 1:1) to obtain the desired compound (0.44 g, yield: 76.2%) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05594154 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-58df597f495940dda9f2b60e6efab7b3 |
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| Source note | uspto-grants-1997_01 |
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