HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059065Generated: October 26, 2026
4-Isobutylbenzoic acid → (4-Isobutylphenyl)(phenyl)methanone
https://huagongshe.com/reaction/1059065
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Isobutylbenzoic acid | HCID 38111 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Isobutylphenyl)(phenyl)methanone | HCID 12158286 | 81% |
Reaction Steps
A solution of 4-isobutylbenzoic acid (5.00 g, 28.0 mmol) in CH2Cl2 was cooled in an ice bath and treated with oxalyl chloride (5 mL) and DMF (1 drop). The mixture was warmed to room temp and stirred 1 h. The volatiles were removed in vacuo to give the crude acid chloride which as dissolved in benzene (50 mL). Aluminum chloride (4.49 g, 33.3 mmol) was added and the mixture was heated to reflux for 3.5 h. The mixture was cooled to room temp and then poured onto ice (ca. 100 g). The mixture was extracted with EtOAc (3×100 mL) and the combined organic extracts were washed with ½ satd aqueous NaHCO3 (100 mL), dried (Na2SO4), filtered and evaporated in vacuo. The resulting residue was purified by silica gel chromatography (elute with 10:1 hexane/EtOAc) to give 4-isobutylbenzophenone (5.48 g, 81%). 1H NMR (CDCl3) 7.75 (m, 4H), 7.53 (d, 1H), 7.47 (t, 2H), 7.23 (d, 2H), 2.53 (d, 2H), 1.91 (m, 1H), 0.92 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06518424B1 |
|---|
| Source dataset | uspto-grants-2003_02 |
|---|
| ORD ID | ord-48936313db894300b798028ea9202c83 |
|---|
| Source note | uspto-grants-2003_02 |
|---|