HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117634Generated: October 30, 2026
(4-Nitrophenyl)acetic acid → HCID 3522175, compound
https://huagongshe.com/reaction/2117634
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (4-Nitrophenyl)acetic acid | HCID 4661 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 3522175 | HCID 3522175 | — |
Reaction Steps
4-Nitrophenylacetic acid (2.00 g, 0.011 mol) was dissolved in anhydrous THF (20 mL) with gradual addition of thionyl chloride (1.03 mL, 0.0143 mol) and a catalytic amount of DMF (2 drops) at room temperature and stirred for 24 h. On completion, the reaction was quenched in situ with N-methylpiperazine (3.85 g, 0.038 mol) added dropwise in a solution of DCM (20 mL) at room temperature and stirred overnight to give a beige suspension. The solvent was removed in vacuo and the residue partitioned between DCM (30 mL) and sodium hydroxide (1N, 30 mL). The organic layer was washed twice, dried over sodium sulfate and filtered. Removal of the solvent in vacuo the title compound as an amber oil, which solidified on standing. LCMS:2.5 min; Rt 0.82 (m/z 264, M+H+) 98%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442698B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-eb679a379c6d4c13a9db0e8f585e62ad |
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| Source note | uspto-grants-2008_10 |
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