HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587264Generated: November 2, 2026
Dicyclohexylcarbodiimide → HCID 19757567, compound
https://huagongshe.com/reaction/1587264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-Pyrrolidinopyridine | HCID 75567 | — |
| Reactant | 5-Octylthiophene-2-carboxylic acid | HCID 13128271 | — |
| Reactant | HCID 19757561 | HCID 19757561 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19757567 | HCID 19757567 | 61.4% |
Reaction Steps
15 ml of dichloromethane was added to 0.38 g (1.58 mM) of 5-octylthiophene-2-carboxylic acid and 0.42 g (1.58 mM) of 4-[3-(butyldimethylsilyl)propoxy]phenol, followed by stirring at room temperature to the mixture, 0.31 g (1.50 mM) of N,N'-dicyclohexylcarbodiimide (DCC) and 0.02 g of 4-pyrrolidinopyridine were added, followed by stirring for 5 hours at room temperature. The resultant dicyclohexylurea was recovered by filtration, followed by washing with dichloromethane to be added to the filtrate. The resultant dichloromethane solution was condensed into a solid under reduced pressure, followed by purification by silica gel column chromatography (eluent: toluene) and recrystallization from ethanol to obtain 0.45 g of 4-[3-(butyldimethylsilyl)propoxy]phenyl 5-octylthiophene-2-carboxylate (Yield: 61.4 %). ##STR71##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05217645 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-e464c2424f934b7391e0c3c1ddcffe35 |
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| Source note | uspto-grants-1993_06 |
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