HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761452Generated: November 1, 2026
(3-Methoxyphenyl)acetic acid → HCID 21241497, compound
https://huagongshe.com/reaction/1761452
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (3-Methoxyphenyl)acetic acid | HCID 15719 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 21241497 | HCID 21241497 | — |
Reaction Steps
3-Methoxyphenylacetic acid (100 g, 600 mmole) was dissolved in methylene chloride (600 mL) and treated with oxalyl chloride (60 mL) and DMF (1 mL) at room temperature. The mixture was stirred for four hours until gas evolution ceased. The solvent was evaporated and the residue dried under vacuum to remove excess oxalyl chloride. The oil obtained was dissolved in methylene chloride (400 mL). Half of this solution (200 mL, approx. 300 mmole) was cooled in ice and treated with a solution of 1-benzylpiperazine (60 mL, 350 mmole) and triethylamine (30 mL) in methylene chloride (100 mL) dropwise. The mixture was stirred at room temperature for 16 hours. Sodium bicarbonate solution was added and the mixture stirred for 15 minutes. The layers were separated. The organic phase was washed with water, brine, dried over K2CO3 and evaporated to an oil. Wt. 90 g. A small portion was characterized as the hydrochloride, m.p. 229°-231° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04826844 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-fbeaac927f67448c94ae0a4d19c0f742 |
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| Source note | uspto-grants-1989_05 |
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