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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 68549726 | HCID 68549726 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-bromonaphthalen-2-yl)methanol | HCID 264948 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273885B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-8669f49461d544659887bc2149da102f |
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| Source note | uspto-grants-2012_09 |
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