HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241846Generated: October 25, 2026
Hydrochloric Acid → 4-t-Butyl-2-(4-t-butylbenzoyl)benzoic acid
https://huagongshe.com/reaction/2241846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-Butylbenzene | HCID 7366 | — |
| Reactant | 4-tert-Butylphthalic anhydride | HCID 122930 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-t-Butyl-2-(4-t-butylbenzoyl)benzoic acid | HCID 7730272 | 64% |
Reaction Steps
Added into a 500 ml three-necked flask under the environment of argon were 4-t-butylphthalic anhydride 36 g (176 mmole), t-butylbenzene 27 g (200 mmole) and dichloroethane 100 ml. The mixture was cooled to 0° C. Aluminum chloride 56 g (420 mmole) was added gradually to them. After the addition, they were stirred at room temperature overnight. After the reaction, ice was added gradually followed by the addition of concentrated hydrochloric acid. After the precipitates were filtered, they were thoroughly washed to give the benzoic acid substance 32 g (yield 64%, white powder).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07670506B1 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-8044212375034425a9fa8f3f91130488 |
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| Source note | uspto-grants-2010_03 |
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