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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390891Generated: October 28, 2026

Aluminum(III) Chloride → (3-bromonaphthalen-2-yl)methanol

https://huagongshe.com/reaction/2390891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantAzane;hydrateHCID 12896473—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 68549726HCID 68549726—
SolventTetrahydrofuranHCID 8028—
Product(3-bromonaphthalen-2-yl)methanolHCID 26494867%

Reaction Steps

To the mixture of lithium aluminum hydride (430 mg, 9.0 mmol) and tetrahydrofuran (15 ml) under nitrogen atmosphere, aluminum chloride (1.7 g, 13 mmol) was added at 0° C. (an outer temperature), and the obtained reaction mixture was stirred at the same temperature for 1 hour. Subsequently, 3-bromo-naphthalene-2-carboxylic acid ethyl ester (500 mg, 1.8 mmol) was added to the reaction mixture at 0° C. (an outer temperature), and the reaction mixture was stirred at the same temperature for 1.5 hours. 28% ammonia water was added to the reaction mixture, followed by filtration with Celite. The solvents were evaporated under reduced pressure from the filtrate, and then the obtained residue was purified with NH-silica gel column chromatography (heptane:ethyl acetate=3:1), thereby obtaining the entitled compound (280 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273885B2
Source datasetuspto-grants-2012_09
ORD IDord-8669f49461d544659887bc2149da102f
Source noteuspto-grants-2012_09