HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010722Generated: October 30, 2026
4-Aminophenylacetic acid → HCID 67021624, compound
https://huagongshe.com/reaction/1010722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminophenylacetic acid | HCID 14533 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Product | HCID 67021624 | HCID 67021624 | — |
Reaction Steps
A mixture of 1.5 ml of 2-nitrofluorobenzene (Aldrich), 1.44 g of 4-aminophenyl acetic acid and 0.550 g of KF is stirred at 170° C. for 16 hours in a sealed tube. The mixture obtained is allowed to cool to rt, triturated in CH2Cl2/MeOH (95:5) and filtered. The filtrate obtained is concentrated and the concentrate obtained is purified by silica gel column chromatography. [4-(2-Nitro-phenylamino)-phenyl]-acetic acid is obtained in the form of a solid: ES-MS: 273.0 [M+H]+; single peak at tR=4.44 min (System 1); Rf=0.20 (CH2Cl2/MeOH, 95:5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977338B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-ee93fe5c6c454020964361fb7fd60282 |
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| Source note | uspto-grants-2011_07 |
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