HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607398Generated: October 26, 2026
Water → 2-Cinnamyl-2-(1-naphthylmethyl)malonic acid diethyl ester
https://huagongshe.com/reaction/1607398
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromomethylstyrene | HCID 98116 | — |
| Reactant | Diethyl (1-naphthyl)methylmalonate | HCID 9972002 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-Cinnamyl-2-(1-naphthylmethyl)malonic acid diethyl ester | HCID 53977357 | 76.9% |
Reaction Steps
To a solution of 1.50 g of 2-(1-naphthylmethyl)malonic acid diethyl ester in 20 ml of 1,2-dimethoxyethane was added 0.3 g of a 50% sodium hydride (suspension in oil) under cooling, and then the mixture was stirred for 1 hour. To the mixture was added 1.18 g of cinnamyl bromide, and the mixture was heated under reflux for 5 hours. After cooling, water was added to the reaction mixture, and the mixture was extracted with diethyl ether. The ethereal layer was washed with a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate. The ethereal layer was concentrated under reduced pressure, and the residue was purified by silica gel flash column chromatography (eluent: benzene/hexane=1/1 by volume) to obtain 1.6 g of 2-cinnamyl-2-(1-naphthylmethyl)malonic acid diethyl ester as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04863904 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-fe92e9f63d6b4bfcac2f1680ff6d49a3 |
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| Source note | uspto-grants-1989_09 |
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