Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165157Generated: October 26, 2026

Water → (7-Methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methanol

https://huagongshe.com/reaction/2165157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 7-methoxy-1,2,3,4-tetrahydro-2-naphthalenecarboxylateHCID 54368774—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(7-Methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methanolHCID 10797825—

Reaction Steps

A solution of 23.43 g (100 mmol) of 7-methoxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid ethyl ester in 160 ml of absolute tetrahydrofuran is added dropwise, over a period of 30 minutes, while stirring at room temperature, to a suspension of 3.79 g (100 mmol) of lithium aluminium hydride in 160 ml of absolute diethyl ether. After stirring at room temperature for 1 hour, 3.8 ml of water, 3.8 ml of sodium hydroxide solution (15%) and 11.4 ml of water are added to the reaction mixture. The resulting precipitate is filtered off with suction and the filtrate is concentrated to dryness by evaporation in vacuo. The oily residue is dissolved in diethyl ether, washed with water, dried with sodium sulphate and concentrated to dryness by evaporation. 7-methoxy-1,2,3,4-tetrahydro-naphthalene-2-methanol is obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939160
Source datasetuspto-grants-1990_07
ORD IDord-f9243f24a0c54d56a6157720f598b2b9
Source noteuspto-grants-1990_07