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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328885Generated: October 31, 2026

1-Naphthol → HCID 13055702, compound

https://huagongshe.com/reaction/328885

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 2N-NaOH aqueous solution and then with water. The liquor was dried over anhydrous 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 numberUS04018824
Source datasetuspto-grants-1977_04
ORD IDord-57e0804322d142c0a0c4f9d760ee75fd
Source noteuspto-grants-1977_04