HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292341Generated: October 30, 2026
Acetyl chloride → 2-Methoxy-4-(1-acetyl-4-piperidyloxy)benzoic acid
https://huagongshe.com/reaction/1292341
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methoxy-4-(4-piperidyloxy)benzoic acid | HCID 18914167 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methoxy-4-(1-acetyl-4-piperidyloxy)benzoic acid | HCID 18914145 | — |
Reaction Steps
2-Methoxy-4-(4-piperidyloxy)benzoic acid (0.6 g, 2.09 mmol) was stirred in THF (10 ml) and treated with triethylamine (0.29 ml, 0.21 g, 2.08 mmol), followed by acetyl chloride (0.18 ml, 0.2 g, 2.5 mmol) and an additional 0.35 ml of triethylamine. The mixture was stirred at ambient temperature for 18 hours, then concentrated in vacuo. The residue was partitioned between aqueous sodium bicarbonate and ethyl acetate. The ethyl acetate layer was extracted with sodium bicarbonate solution. The combined sodium bicarbonate layers were acidified with 1N HCl and extracted with ethyl acetate. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered, and evaporated to dryness in vacuo to give 2-methoxy-4-(1-acetyl-4-piperidyloxy)benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05756504 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-6452c7e7aca84e7790de4840c3b9d440 |
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| Source note | uspto-grants-1998_05 |
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