HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330843Generated: October 30, 2026
Furfuryl Alcohol → HCID 56928393, compound
https://huagongshe.com/reaction/330843
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Furfuryl Alcohol | HCID 7361 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | HCID 66693725 | HCID 66693725 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 56928393 | HCID 56928393 | — |
Reaction Steps
To 0.015 g (0.15 mmol) furan-2-ylmethanol in 0.75 mL THF are added 0.03 g (0.10 mmol) N-Ethyl-2-[4-(4-hydroxy-phenylethynyl)-phenyl]-propionamide (XVIII.2) and 40 mg polymer-bound triphenylphosphine (3 mmol/g resin). The mixture is cooled to 0° C. and 0.03 g (0.15 mmol) di-tert-butyl azodicarboxylate dissolved in 0.5 mL THF are added. The mixture is stirred over night at rt. After that time additional 0.03 g (0.15 mmol) di-tert-butyl azodicarboxylate dissolved in 0.5 mL THF are added and stirring is continued over night. Subsequently the mixture is filtered (Alox), washed (DMF/MeOH 9:1) and concentrated. The residue is dissolved in DMF and the desired product was purified using RP-HPLC (narrow gradient, water/MeOH+0.1% TFA).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877754B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3dc897e7c99d4f3ba11d71ea75107495 |
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| Source note | uspto-grants-2014_11 |
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