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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606696Generated: November 2, 2026

Triethylamine → 1-Methoxy-3-(1,2,3,4-tetrahydro-1-naphthyl)urea

https://huagongshe.com/reaction/1606696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant1-Isocyanato-1,2,3,4-tetrahydronaphthaleneHCID 16217239—
SolventDichloromethaneHCID 6344—
Product1-Methoxy-3-(1,2,3,4-tetrahydro-1-naphthyl)ureaHCID 2139348676.6%

Reaction Conditions

Temperature15 °C

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. Analysis Calculated for C12H16N2O2 : C, 65.43; H, 7.32; N, 12.72. Found: C, 65.32; H, 7.33; N, 12.64.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953506
Source datasetuspto-grants-1976_04
ORD IDord-482ebdd128344af39fc77f9f9c5adfad
Source noteuspto-grants-1976_04