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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720672Generated: November 2, 2026

Formaldehyde → HCID 11776435, compound

https://huagongshe.com/reaction/1720672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantNSC112269HCID 270093—
ReactantLithium ChlorideHCID 433294—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11776435HCID 11776435—

Reaction Steps

1.92 g of lithium chloride was suspended-in 50 ml of dry THF, and 15 g of ethyl 2-diethylphosphono-3-(1-naphthyl)propionate was dropwise added thereto. Then, 16 ml of a 50% dry THF solution of DBU was dropwise added thereto, and 2.01 g of paraformaldehyde suspended in dry THF was added thereto. The mixture was stirred at room temperature for 3 hours, and the insolubles were removed by filtration and washed with a small amount of diethyl ether. The washing solution and and the filtrate were put together, and the solvent was distilled off. The resulting syrup was dissolved in 180 ml of diethyl ether. The diethyl ether layer was washed sequentially with a 10% citric acid aqueous solution, with water and with a saturated sodium chloride aqueous solution and dried over anhydride sodium sulfate. The solvent was distilled off, and the syrup thereby obtained was purified by silica gel column chromatography (n-hexane/diethyl ether=20/1) to obtain 6.48 g of ethyl 2-(1-naphthyl)methyl-2-propenoate as colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506356
Source datasetuspto-grants-1996_04
ORD IDord-598ffbb2a52d42c881e6a0ee975d2a3b
Source noteuspto-grants-1996_04