Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703872Generated: October 31, 2026

Cyclohexanone → HCID 15617826, compound

https://huagongshe.com/reaction/703872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
Reactant1-(methoxymethoxy)naphthaleneHCID 10779684—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 15617826HCID 1561782658%

Reaction Steps

A solution of 1-methoxymethoxy-naphthalene (3.76 g, 0.020 mole) in dry ether (40 mL) was treated with n-butyllithium (1.6M in hexane: 25.0 mL, 0.040 mole) at room temperature over a period of 15 minutes. After stirring for an additional 1.5 hours, a solution of cyclohexanone (4.90 g, 0.050 mole) in either (15 mL) was added and the resulting mixture was stirred at room temperature for 2 hours. It was then quenched with saturated aqueous ammonium chloride and the crude product was isolated by extraction with ether. Chromatography with 9:1 hexane/ethyl acetate provided the title compound as a colorless oil (3.30 g, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985442
Source datasetuspto-grants-1991_01
ORD IDord-351b5d1b11794fe988bd3c65f1b77d17
Source noteuspto-grants-1991_01