HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129338Generated: October 29, 2026
Tetrahydrofuran → HCID 15023382, compound
https://huagongshe.com/reaction/129338
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | HCID 15023289 | HCID 15023289 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | HCID 15023382 | HCID 15023382 | 73% |
Reaction Steps
To 25 ml of tetrahydrofuran were added 1.50 g (5.11 mmol) of 5-tridecylpyrrole-3-carboxylic acid and 1.27 g (6.15 mmol) of dicyclohexylcarbodiimide, followed by adding 3.8 ml of n-propyl alcohol and 62 mg of dimethylaminopyridine. Then the mixture was heated at 60° C. for 10 hours under stirring. After cooling, the resulting precipitates were filtered off and washed well with ether. The filtrate and the washing liquid were combined and concentrated. The residue was purified by subjecting it to column chromatography over silica gel (eluent: ethyl acetate/hexane=1/20) to obtain 1.26 g (73% yield) of propyl 5-tridecylpyrrole-3-carboxylate, m.p. 51°-52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE035096 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-453226edff9a4a799c19e7680f0d34af |
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| Source note | uspto-grants-1995_11 |
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