HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249635Generated: November 2, 2026
Oxalyl chloride → 5-(2,4-Diisobutoxybenzoyl)-2-isobutoxyphenyl acetate
https://huagongshe.com/reaction/2249635
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 1,3-Diisobutoxybenzene | HCID 13087565 | — |
| Reactant | 3-(Acetyloxy)-4-isobutoxybenzoic acid | HCID 17816473 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(2,4-Diisobutoxybenzoyl)-2-isobutoxyphenyl acetate | HCID 17816457 | 68.5% |
Reaction Steps
In 10 ml of methylene chloride is dissolved 1.00 g of 3-(acetyloxy)-4-isobutoxybenzoic acid. After adding 0.41 ml of oxalyl chloride and 20 μl of N,N-dimethylformamide successively at ambient temperature, the mixture thus obtained is stirred at ambient temperature for one hour. Then, 1.06 g of aluminum chloride and 1.15 g of 1,3-diisobutoxybenzene are successively added at 5-10° C., and the mixture is stirred at the same temperature as above for one hour. The reaction mixture is added to a mixture of methylene chloride and ice water, and the organic layer is separated. The organic layer is successively washed with water and saturated aqueous solution of sodium chloride 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; n-hexane:ethyl acetate=5:1] to obtain 1.24 g of 5-(2,4-diisobutoxybenzoyl)-2-isobutoxyphenyl acetate as a yellow 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-ea17877cfbc14e52943175709ae06e5a |
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| Source note | uspto-grants-2008_01 |
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