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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348735Generated: October 30, 2026

Methanol → 3-(6-t-Butyldimethylsilyloxymethylnaphthalen-2-yl)propan-1-ol

https://huagongshe.com/reaction/348735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-(6-t-butyldimethylsilyloxymethylnaphthalen-2-yl)propionic Acid Methyl EsterHCID 66941531—
SolventTetrahydrofuranHCID 8028—
Product3-(6-t-Butyldimethylsilyloxymethylnaphthalen-2-yl)propan-1-olHCID 23079169109.3%

Reaction Steps

The compound (2.62 g) obtained in Example 121-5 was dissolved in anhydrous THF (100 ml) and added with lithium aluminum hydride (555 mg) under ice-cooling, followed by stirring for 30 minutes under a nitrogen atmosphere. After completion of the reaction, the solution was added with methanol and then added with an aqueous potassium sodium tartrate solution, followed by stirring overnight. The solution was extracted with chloroform and the extract was washed with saturate saline solution. Then, the organic layer was dried with anhydrous sodium sulfate. The solvent was distilled off, thereby obtaining the subject compound (2.64 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176227B2
Source datasetuspto-grants-2007_02
ORD IDord-e6fe9df5ce3449bebf2a11a3b6d20ed7
Source noteuspto-grants-2007_02