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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051089Generated: October 25, 2026

Ethanol → 2-Tricyclo(3.3.1.13,7)dec-1-yl-1-naphthalenol

https://huagongshe.com/reaction/2051089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant1-NaphtholHCID 7005—
Reactant1-Adamantyl acetateHCID 519973—
SolventCyclohexaneHCID 8078—
Product2-Tricyclo(3.3.1.13,7)dec-1-yl-1-naphthalenolHCID 1983450820.7%

Reaction Steps

A three-necked 100 ml flask is charged with 2.7 g of 1-acetoxyadamantane and 5 ml of cyclohexane in a nitrogen atmosphere. After complete dissolution, there are introduced 1.4 g of concentrated sulfuric acid. In a single portion there is added a suspension of 2 g of 1-naphthol in 15 ml of cyclohexane and one agitates for 45 minutes. 20 ml of ethanol are added and the mixture is filtered. One washes the residue with ethanol and with water and dries on the filter. After recrystallization with cyclohexane, one obtained 0.8 g of the desired product melting at 209.2°-209.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015758
Source datasetuspto-grants-1991_05
ORD IDord-62f4e1c95f6c48939dd75d78f8726d6f
Source noteuspto-grants-1991_05