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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461379Generated: October 30, 2026

3-(2-Chloroethyl)-1-(1,2,3,4-tetrahydro-1-naphthyl)urea → HCID 21393499, compound

https://huagongshe.com/reaction/461379

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Chloroethyl)-1-(1,2,3,4-tetrahydro-1-naphthyl)ureaHCID 98980—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21393499HCID 2139349921.6%

Reaction Steps

To a stirred solution of 3.8 grams (0.015 mole) of 1-(2-chloroethyl)-3-(1,2,3,4-tetrahydro-1-naphthyl)urea in 75 ml. dry tetrahydrofuran is added dropwise a solution of 2.25 grams (0.02 mole) of potassium tert-butoxide in 50 ml. of dry tetrahydrofuran under a nitrogen atmosphere. The reaction is then allowed to proceed at ambient temperature overnight. The mixture is then evaporated at reduced pressure. The residue is partitioned between water and ether. The ether layer is washed with water, dried, sodium sulfate, and evaporated at reduced pressure. Crystallization of the residue from acetone-ether-hexane gives 0.70 grams of product, melting point 134° to 139.5° C. Recrystallization from acetone-hexane gives the analytical sample, melting point 138° to 141.5° C. Analysis calculated for C13H16N2O: C, 72.19; H, 7.46; N, 12.95. Found: C, 72.04; H, 7.43; N, 12.89.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04062856
Source datasetuspto-grants-1977_12
ORD IDord-dad4ee5766ff44d980668c7d84a0a7c6
Source noteuspto-grants-1977_12