HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249631Generated: November 3, 2026
Oxalyl chloride → Ethyl 3-[5-(2,5-diisobutoxybenzoyl)-2-isobutoxyphenyl]propanoate
https://huagongshe.com/reaction/2249631
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Ethyl 3-(2-isobutoxyphenyl)propanoate | HCID 17816468 | — |
| Reactant | 2,5-Diisobutoxybenzoic acid | HCID 17816477 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-[5-(2,5-diisobutoxybenzoyl)-2-isobutoxyphenyl]propanoate | HCID 17816548 | 98.4% |
Reaction Steps
In 50 ml of methylene chloride is dissolved 5.00 g of 2,5-diisobutoxybenzoic acid. After adding 2.0 ml of oxalyl chloride and subsequently 20 μl of N,N-dimethylformamide at ambient temperature, the mixture thus obtained is stirred at ambient temperature for one hour. Then, 7.51 g of aluminum chloride and subsequently 5.17 g of ethyl 3-(2-isobutoxyphenyl)-propanoate are added at −30° C., the mixture thus obtained is stirred at −10° C. for 10 minutes. The reaction mixture is added to a mixture of chloroform and ice water and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. The residue thus obtained is purified by silica gel column chromatography (eluent; hexane:ethyl acetate=5:1) to obtain 9.21 g of ethyl 3-[5-(2,5-diisobutoxybenzoyl)-2-isobutoxyphenyl]propanoate as a yellow-colored oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314888B1 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-bceb32f5e26e44adb92a08ab5636c1cd |
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| Source note | uspto-grants-2008_01 |
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