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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424708Generated: October 26, 2026

Water → (1,2,3,4-Tetrahydronaphthalen-1-yl)methanol

https://huagongshe.com/reaction/1424708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant1,2,3,4-Tetrahydro-1-naphthoic acidHCID 12598146—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(1,2,3,4-Tetrahydronaphthalen-1-yl)methanolHCID 11062704100.9%

Reaction Steps

200 mg (1.10 mmol) of 1,2,3,4-tetrahydro-naphthalen-1-carboxylic acid compound was dissolved in 9 mL of tetrahydrofuran, and then 129 mg (3.30 mmol) of lithium aluminum hydride was added at 0° C. and stirred at room temperature for 1 hour. Water was slowly added to quench the reaction, and when a gel was formed by adding ethyl acetate, the celite was filtered. Then, the residue was dissolved again in 20 mL of ethyl acetate and the organic layer was washed with distilled water three times. The organic layer was dried with anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure to give 180 mg of colorless oil (yield: 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927760B2
Source datasetuspto-grants-2015_01
ORD IDord-fd5b3c7e23494a7387d9310c75d43ddc
Source noteuspto-grants-2015_01