HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544714Generated: October 30, 2026
Dicyclohexylcarbodiimide → 5-chloro-6-(piperidin-1-yl)-benzofuran-2(3H)-one
https://huagongshe.com/reaction/544714
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 5-Chloro-2-hydroxy-4-(piperidin-1-yl)-phenylacetic acid | HCID 53913044 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-chloro-6-(piperidin-1-yl)-benzofuran-2(3H)-one | HCID 13576952 | — |
Reaction Steps
A solution of 6.5 g (31.5 mmoles) of dicyclohexylcarbodiimide in 40 ml of absolute methylene chloride is added at room temperature in the course of approximately 3 minutes to a solution of 8.1 g (30 mmoles) of crude 5-chloro-2-hydroxy-4-(piperidin-1-yl)-phenylacetic acid in 50 ml of absolute methylene chloride. The reaction mixture is stirred at room temperature for 30 minutes. The precipitated dicyclohexylurea is filtered off with suction and washed with methylene chloride. The filtrate is concentrated by evaporation in a vacuum rotary evaporator and the residue is chromatographed over silica gel with the eluant methylene chloride/hexane (1:1). Recrystallisation from hexane yields 5-chloro-6-(piperidin-1-yl)-benzofuran-2(3H)-one having a melting point of 129°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04451462 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-651c7a7cd4f84285988f9a7cb5b05936 |
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| Source note | uspto-grants-1984_05 |
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