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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248162Generated: October 31, 2026

Water → L 646462

https://huagongshe.com/reaction/1248162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantHexamethylphosphoramideHCID 12679—
ReactantHCID 12909376HCID 12909376—
ProductL 646462HCID 145990—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 1.0 g (0.00302 mole) of (±)-5-(1-methyl-4-piperidylidene)-5H-dibenzo[a,d]-cycloheptene-3-carboxylic acid, 0.31 g (0.0030 mole) of triethylamine and 4 ml of hexamethylphosphoramide was added 0.456 g (0.0030 mol) of 1H-1-chloromethyl-3-methyl-2,5-dioxo-2,3,4,5-tetrahydroimidazole. The mixture was stirred and heated in an oil bath at 100° C. for 18 hours. After cooling, 25 ml of water and 25 ml of a saturated solution of sodium carbonate were added to the reaction. The mixture then was extracted with ten 50 ml aliquots of ether. The combined ether extracts were washed with ten 75 ml portions of water, dried over magnesium sulfate, filtered, and the solvent was removed on a rotary evaporator. The white crystalline residue was recrystallized from acetonitrile to afford (±)-(3-methyl-2,5-dioxo-1-imidazolidinyl)methyl 5-(1-methyl-4-piperidinylidene)-5H-dibenzo[a,d]cycloheptene-3-carboxylate, m.p. 192°-194°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522821
Source datasetuspto-grants-1985_06
ORD IDord-77b364262c664c08a58dbb23152c33c1
Source noteuspto-grants-1985_06