HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606787Generated: November 2, 2026
Triethylamine → 1-Methoxy-3-(1,2,3,4-tetrahydro-1-naphthyl)urea
https://huagongshe.com/reaction/1606787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 1-Isocyanato-1,2,3,4-tetrahydronaphthalene | HCID 16217239 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Methoxy-3-(1,2,3,4-tetrahydro-1-naphthyl)urea | HCID 21393486 | 76.6% |
Reaction Steps
To an ice-cold, stirred mixture of 6.7 grams (0.080 mole) of methoxyamine hydrochloride in 80 ml of methylene chloride is added a solution of 8.1 grams (0.080 mole) of triethylamine in 20 ml of methylene chloride. The mixture is stirred at 15°C. for 15 minutes, and is then allowed to warm to 15°C. to 25°C. while a solution of 6.94 grams (0.04 mole) of 1,2,3,4-tetrahydro-1-naphthyl isocyanate in 25 ml of methylene chloride is added dropwise. The mixture is stirred for 30 minutes at room temperature and then filtered. The filtrate is washed with water, dried (sodium sulfate), and the solvent evaporated at reduced pressure to give a solid. Recrystallization of the solid from acetone/hexane gives 6.75 grams of the product, melting point 122°C. to 125°C. Recrystallization of the product from acetone/hexane gives the analytical sample, melting point 123.5°C. to 125°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03953606 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-5bd89e8ccb354e7da4b38b1d2f425c0a |
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| Source note | uspto-grants-1976_04 |
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