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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623039Generated: October 29, 2026

Naphthalene → (8-Methylnaphthalen-1-yl)methanol

https://huagongshe.com/reaction/1623039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNaphthaleneHCID 931—
ReactantNaphthalanHCID 588214—
ReactantPotassiumHCID 5462222—
SolventTetrahydrofuranHCID 8028—
Product(8-Methylnaphthalen-1-yl)methanolHCID 15618201—

Reaction Conditions

Temperature60 °C

Reaction Steps

A 3-L 4-neck flask equipped with an overhead stirrer, a thermocouple, a condenser, a nitrogen inlet, and a 1-L addition funnel was charged with potassium (30 g, 0.764 mol) and THF (1 L). The metal suspension was heated to 60° C. for 30 min and then stirred to room temperature. To the reaction mixture was then added naphthalene (2 g, 0.015 mol), the suspension was stirred at room temperature for 10 min and then cooled to −20° C. to afford a blue suspension. A solution of 1H,3H-Benzo[de]isochromene (26 g, 0.153 mol) in THF (500 ml) was slowly added via the addition funnel, with addition controlled so that the reaction temperature did not exceed −15° C. After stirring for 5 h at −20° C., the suspension was removed from the cooling bath, warmed with stirring to 0° C., and then allowed to stand without stirring (potassium metal settling). The solution was decanted and the residual potassium was cooled and carefully decomposed with isopropyl alcohol (IPA) under N2. The decanted solution was carefully treated with water (20 mL) under nitrogen and stirring was continued for 20 min. Additional water and ether were added and the organic layer was separated. The aqueous layer was extracted with CH2Cl2 and the combined organics were dried over MgSO4 and condensed in vacuo to yield a crude material. The crude material was purified by flash chromatography (7.5/2.5 hexane/EtOAc) to yield 8-methyl-1-napthalenemethanol as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778956B2
Source datasetuspto-grants-2014_07
ORD IDord-56435e4300ba4d98984f4dd002e2ea49
Source noteuspto-grants-2014_07