HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720313Generated: October 29, 2026
Triethyl phosphonoacetate → Ethyl 3-(5,6,7-trimethoxynaphthalen-2-yl)propenoate
https://huagongshe.com/reaction/720313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5,6,7-Trimethoxynaphthalene-2-carbaldehyde | HCID 21891637 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 3-(5,6,7-trimethoxynaphthalen-2-yl)propenoate | HCID 68436859 | — |
Reaction Steps
55% Sodium hydride (241 mg) was suspended in THF (2.5 mL) at −10° C. under an argon atmosphere, a solution of ethyl diethylphosphonoacetate (1.23 g) in THF (5 mL) was added dropwise to the suspension, and the mixture was stirred for 30 minutes. A solution of 5,6,7-trimethoxynaphthalene-2-carboaldehyde (1.23 g) in THF (10 mL) was then added dropwise, and the mixture was stirred for 30 minutes at −10° C. and 1 hour at room temperature. The reaction mixture was diluted with ethyl acetate, washed with 2 M hydrochloric acid, water and saturated brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:2) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135473B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-09db1d04b4fb45d4926a8b44684d8d97 |
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| Source note | uspto-grants-2006_11 |
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