HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209641Generated: October 29, 2026
Aluminum(III) Chloride → HCID 19420759, compound
https://huagongshe.com/reaction/2209641
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 19420771 | HCID 19420771 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19420759 | HCID 19420759 | — |
Reaction Steps
Aluminum chloride (0.2 g; 1.5 mmol) is added to a suspension of lithium aluminum hydride (60 mg; 1.5 mmol) in dry ether (6 ml) at 0° C. The reaction is stirred for 10 minutes at 20° C. and cooled to 0° C. A solution of 4-(benzoxazol-2-yl)benzyl cyanide (0.24 g; 1.02 mmol) in dry THF (4 ml) is added dropwise and the reaction is stirred at 20° C. for 2 hours. The reaction is quenched with H2O, diluted with ether and washed vigorously with 2N HCl. The ether is decanted and the aqueous layer is washed with ether. The aqueous phase is neutralized with 15% NaOH and extracted with CH2Cl2. The extracts are concentrated and purified with column chromatography using CH2Cl2 to 20% MeOH/CH2Cl2. The product is acidified with acidic methanol and concentrated to yield 2-[4-(benzoxazol-2-yl)phenyl]- 1-ethanamine hydrochloride (m.p. 250° C. dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05455260 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-d11ba0b096e44b608fe4e810efe73a72 |
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| Source note | uspto-grants-1995_10 |
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