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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198836Generated: November 2, 2026

1-Naphthol → HCID 13055702, compound

https://huagongshe.com/reaction/2198836

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphtholHCID 7005—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Ethylazetidin-3-olHCID 13813928—
ProductHCID 13055702HCID 1305570270%

Reaction Conditions

Temperature160 °C

Reaction Steps

To a mixture of 10.2 parts of 1-ethyl-3-azetidinol and 14.4 parts of α-naphthol 0.2 part of potassium hydroxide was added, and the mixture was heated under nitrogen gas at 160° C. for 18 hours. The reaction mixture was cooled and extracted with ether. The ether extract was washed with 2 N-NaOH aqueous solution and then with water. The liquor was dried over anhydride sodium sulfate and the solvent was distilled off. The residue was recrystallized from cyclohexane to yield 17.2 parts of 1-(α-naphthoxy)-3-ethylamino-2-propanol. The melting of the product was 106°-107° C. The yield was 70%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04360464
Source datasetuspto-grants-1982_11
ORD IDord-07abf7f93f334df4a069eaad88f5ac07
Source noteuspto-grants-1982_11