HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636306Generated: October 30, 2026
Aluminum(III) Chloride → HCID 18518301, compound
https://huagongshe.com/reaction/636306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 12743495 | HCID 12743495 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 18518301 | HCID 18518301 | — |
Reaction Steps
A solution of 2-benzyl-4-methoxyphenylacetic acid (14.2 g, 0.055 m) in benzene (120 mL) and thionyl chloride (28 mL) was refluxed for 1 hour and concentrated. The acid chloride was dissolved in dry methylene chloride (40 mL), and the solution was added dropwise under argon to a solution of AlCl3 (14.7 g, 0.11 mol) in methylene chloride (600 mL). The reaction was stirred under an argon atmosphere for 2.5 hours at room temperature, then was quenched with ice-water (200 mL). The layers were separated, and the organic phase was washed sequentially with 10% NaOH solution, water, and dil. HCl. The resulting solution was diluted with ether (200 mL), dried over MgSO4, and concentrated. The solid residue was triturated with ether/hexane (1:1) and 9.35 g of the title compound was collected by filtration: Mp 105-106° C.; 1H NMR (400 MHz, CDCl3) δ 3.72 (s, 3H), 4.1 (s, 2H), 4.2 (s, 2H), 6.7 (d, 1H), 6.82 (s, 1H), 7.30 (m, 4H), 8.1 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06191304B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-43b10ea66eeb418083aeba47bba2061a |
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| Source note | uspto-grants-2001_02 |
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