HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604742Generated: October 31, 2026
Hydrochloric Acid → HCID 20306642, compound
https://huagongshe.com/reaction/604742
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 4-Methoxy-2-methylbenzoic acid | HCID 597216 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Catalyst | Oxalyl chloride | HCID 65578 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20306642 | HCID 20306642 | 59.1% |
Reaction Steps
Oxalyl chloride (3.43 mL, 0.0400 mmol) and N,N-dimethylformamide (2 drops) were added to chloroform (60 mL) solution of 4-methoxy-2-methylbenzoic acid (5.0 g, 0.0300 mol). After the reaction mixture was stirred at room temperature for one hour, the reaction solvent was evaporated under reduced pressure. The obtained yellow oily substance was dissolved in chloroform (60 mL). Toluene (3.52 mL, 0.0330 mol) and aluminum chloride (8.02 g, 0.0601 mol) were added to this solution while cooled on ice, and the reaction mixture was stirred for three and a half hours while keeping the reaction mixture cooled ice. After 5% hydrochloric acid was added to the reaction mixture and extracted with chloroform, the organic phase was washed with 10% hydrochloric acid, water, a saturated sodium bicarbonate aqueous solution and brine, and dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the residue obtained by evaporating the solvent under reduced pressure was purified by silica gel column chromatography (hexane:ethyl acetate=15:1) to obtain yellow oily (4-methoxy-2-methylphenyl) (4-methylphenyl)methanone (4.26 g, 58.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910619B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-610802ab67504ae0afcd575d2c09c7db |
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| Source note | uspto-grants-2011_03 |
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