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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330843Generated: October 30, 2026

Furfuryl Alcohol → HCID 56928393, compound

https://huagongshe.com/reaction/330843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuryl AlcoholHCID 7361—
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
ReactantHCID 66693725HCID 66693725—
SolventTetrahydrofuranHCID 8028—
ProductHCID 56928393HCID 56928393—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877754B2
Source datasetuspto-grants-2014_11
ORD IDord-3dc897e7c99d4f3ba11d71ea75107495
Source noteuspto-grants-2014_11