HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398897Generated: October 31, 2026
Dicyclohexylcarbodiimide → HCID 68121019, compound
https://huagongshe.com/reaction/2398897
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-(Piperidin-1-yl)butanoic acid hydrochloride | HCID 13172081 | — |
| Reactant | HCID 54306291 | HCID 54306291 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68121019 | HCID 68121019 | — |
Reaction Steps
2.5 g. (6.76 mmole) of 3-(4-fluorophenyl-1-methylbutyl)-1-hydroxy-6,6,9-trimethyl-7,8,9,10-tetrahydro-6H-dibenzo[b,d]pyran is combined with 1.41 g. (6.76 mmole) of γ-piperidinobutyric acid hydrochloride and 1.48 g. (7.16 mmole) of dicyclohexylcarbodiimide in 125 ml. of methylene chloride and stirred at room temperature for 16 hours. The by-product of dicyclohexylurea is removed by filtration and the filtrate is evaporated to a residue. The residue is dissolved in ether and the small amount of solid which appears is removed by filtration. The ether is removed on a rotary evaporator and the gummy residue which remains is triturated several times with small quantities of hexane. The material is thoroughly dried to yield the product as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04025630 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-3ff761837ab34e268e0a5a02f81793b9 |
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| Source note | uspto-grants-1977_05 |
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