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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346277Generated: October 29, 2026

Hydrochloric Acid → HCID 14726488, compound

https://huagongshe.com/reaction/346277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl terephthalateHCID 8441—
ReactantSodium hydrideHCID 24758—
Reactant1-(5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)ethan-1-oneHCID 2747562—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 14726488HCID 1472648856.3%

Reaction Steps

A solution of 19.4 g (0.1 mole) of dimethyl terephthalate and 23 g (0.1 mole) of 6-acetyl-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene in a mixture of 80 ml of toluene and 20 ml of dimethoxyethane was added dropwise at 100° C. to a suspension of 6.3 g (0.15 mole) of sodium hydride in 21 ml of toluene under nitrogen. The reaction mixture was refluxed with stirring for 5 hours and then cooled, after which 50 ml of water were added and the mixture was acidified with semiconcentrated hydrochloric acid, poured onto 500 ml of water and extracted with chloroform. The product which had already precipitated was filtered off under suction, and the chloroform phase was dried over sodium sulfate and evaporated down. The residue and the crude product filtered off under suction beforehand were combined and were extracted several times with hot methanol. After the remaining crystals had been dried, 22.1 g of 1-(4-carbomethoxyph-enyl)-3-(5,6,7,8-tetrahydro- 5,5,8,8-tetramethyl-2-naphthalenyl)-propane-1,3-dione of melting point 128° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05061705
Source datasetuspto-grants-1991_10
ORD IDord-68c0f88dc6944bfcbf2ad56e854b7716
Source noteuspto-grants-1991_10