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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105741Generated: October 31, 2026

Diethyl Ether → HCID 57809429, compound

https://huagongshe.com/reaction/2105741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDiethyl methylmalonateHCID 11857—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Bromomethyl)-6-methylnaphthaleneHCID 12337302—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57809429HCID 5780942981%

Reaction Steps

To a stirred suspension of 3.6 g NaH (90 mmol, 60% in mineral oil) in 200 ml Et2O 16.2 ml (94 mmol) of diethyl 2-methylmalonate was added slowly with cooling. After 2 h stirring at 20 C, solution of 21.2 g (90 mmol) of 2-(bromomethyl)-6-methylnaphthalene (prepared according Buu-Hoi L.; J. Chem. Soc.; 1946; 831) in 30 ml of THF was added, resulting mixture was stirred overnight and decomposed by addition of saturated NH4Cl solution. Organic phase was separated, aqueous—extracted twice with 100 ml portions of ether. Combined extracts were evaporated, residue was dissolved in 150 ml methanol and solution of KOH (20 g, 360 mmol) was added slowly. Mixture was refluxed for 5 h, then evaporated to dryness and resulting semisolid was dissolved in warm water (400 ml). Solution was extracted three times with 100 ml portions of ether, then acidified by carefully addition of 10% HCl. Precipitate of acid 2 was collected and dried, yielded 20 g (81%) of white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579417B2
Source datasetuspto-grants-2009_08
ORD IDord-3f517ca8790d45919ea4db9f41fa22c0
Source noteuspto-grants-2009_08