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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(2-Chloroethyl)-1-(1,2,3,4-tetrahydro-1-naphthyl)urea | HCID 98980 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21393499 | HCID 21393499 | 21.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04062856 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-dad4ee5766ff44d980668c7d84a0a7c6 |
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| Source note | uspto-grants-1977_12 |
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