HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092435Generated: November 2, 2026
Ethylbenzene → (5-Chloro-2-hydroxyphenyl)(4-ethylphenyl)methanone
https://huagongshe.com/reaction/1092435
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylbenzene | HCID 7500 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-Chloro-o-anisic acid | HCID 76970 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (5-Chloro-2-hydroxyphenyl)(4-ethylphenyl)methanone | HCID 57741112 | 71% |
Reaction Steps
A solution of 2-methoxy-5-chlorobenzoic acid (2.0 g, 10.5 mmol) in dry CH2Cl2 (10 mL) was stirred at room temperature under agron. Oxalyl chloride (2.0 g, 15.8 mmol) was added dropwise to the reaction mixture followed by DMF (0.04 mL). After stirring overnight, the volatiles were evaporated using a rotary evaporator and the residue was dissolved in dry CH2Cl2 (10 mL) at room temperature under agron. After cooling to −5° C., ethylbenzene (2.57 mL, 21 mmol) was added, followed by portionwise addition of AlCl3 (2.80 g, 21 mmol) while maintaining the reaction temperature between −5° C. and 0° C. The reaction mixture was stirred for 4 h at room temperature, and then poured into ice water and extracted with CH2Cl2 (50 mL×2). The organic layer was then washed with 1N HCl (50 mL), 1N NaOH (50 mL), water (50 mL) and brine (50 mL) and dried over anhydrous Na2SO4. The filtrate was concentrated and the crude product was purified by column chromatography (PE:EA=10:1) to give the target compound (1.944 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129434B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-42bee6de9b444d489f1e075ac4ea2956 |
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| Source note | uspto-grants-2012_03 |
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