HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488127Generated: October 28, 2026
Water → (E)-3-(5-ethyl-4-hydroxy-3-methoxy-1-naphthyl)-2-methylpropenoic acid
https://huagongshe.com/reaction/488127
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Triethyl 2-phosphonopropionate | HCID 107155 | — |
| Reactant | 5-Ethyl-3-methoxy-4-methoxymethoxy-1-naphthalenecarbaldehyde | HCID 9970569 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-3-(5-ethyl-4-hydroxy-3-methoxy-1-naphthyl)-2-methylpropenoic acid | HCID 6509859 | 122% |
Reaction Steps
36 g of 60% sodium hydride was suspended in 500 ml of N,N-dimethylformamide and 268 g of triethyl 2-phosphonopropionate was added at ice bath temperature. After stirring at room temperature for 1 hour, a solution of 206 g of 5-ethyl-3-methoxy-4-methoxymethoxy-1-naphthalenecarbaldehyde was added. After stirring at room temperature for 15 minutes, ice cooled water was gradually added at ice bath temperature. The mixture was extracted with ethyl acetate and the combined organic layer was washed with brine. After drying over anhydrous magnesium sulfate, the solvent was evaporated and the residue was purified by silica gel column chromatography (10% ethyl acetate/hexane) to obtain 262.4 g of the titled compound as a yellow oil (containing a small amount of Z isomer).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05298649 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-4f1aa77bad7c4150b8651deb1344b99e |
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| Source note | uspto-grants-1994_03 |
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