HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239606Generated: October 29, 2026
Phenylacetic Acid → HCID 12209494, compound
https://huagongshe.com/reaction/239606
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylacetic Acid | HCID 999 | — |
| Reactant | 4-Bromoanisole | HCID 7730 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12209494 | HCID 12209494 | 66% |
Reaction Steps
Phenylacetic acid (1.09 g, 80 mmoles) was dissolved in 5 ml dichloromethane. To this mixture, oxalylchloride (1.01 g, 80 mmoles) and DMF (3 drops) were added at 0° C. and stirred for 30 min. The solvent was evaporated and dissolved in 5 ml dichloromethane. To this mixture, 4-bromoanisole (1 g, 5.34 mmoles) was added and cooled to 0° C. At 0° C. AlCl3 (1.06 g, 80 mmoles) was added and the reaction mixture was warmed to RT and stirred overnight. The reaction mixture was quenched by the addition of 2N HCl and extracted with ethyl acetate, dried over sodium sulphate and concentrated. The crude product was purified by column chromatography to afford the title compound as white solid (1 g, 66% yield). MP: 83-86° C. 1H-NMR (δ ppm, CDCl3, 400 MHz): δ 11.56(s,1H), 8.01(d, J=2.2 Hz, 1H), 7.64(dd, J=8.8, 2.5 Hz, 1H), 7.32(t, 2H), 7.29(m,3H), 6.96(d, J=8.8 Hz,1H), 4.43(s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642607B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-f285e7cff4a542759d4bf90b50d3a01d |
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| Source note | uspto-grants-2014_02 |
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