HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377831Generated: October 26, 2026
Triphenylphosphine → 5-Ethyl-2-[3-[2,6-dimethyl-4-(2-methyl-tetrazol-5-yl)-phenoxy]-propyl]furan
https://huagongshe.com/reaction/1377831
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Win 58768 | HCID 148372 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 5-Ethyl-2-(3-hydroxypropyl)furan | HCID 22915401 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Ethyl-2-[3-[2,6-dimethyl-4-(2-methyl-tetrazol-5-yl)-phenoxy]-propyl]furan | HCID 15954643 | 65.4% |
Reaction Steps
Diethyl azodicarboxylate (DEAD, 4.84 g; 27.8 mmol) was added under nitrogen to a stirred and cooled (-20° C.) solution of triphenylphosphine (7.37 g; 27.8 mmol), 5-ethyl-2-(3-hydroxypropyl)furan (Intermediate 1c) (3.9 g; 25.3 mmol), and 4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenol (5.69 g; 27.8 mmol). The mixture was stirred at -20° C. for 1/2 h, and then was allowed to warm to room temperature overnight. Water (50 mL) was added to the mixture and the layers were separated. The aqueous layer was extracted with ether (3×50 mL), the organic layer was washed with 10% NaOH solution (3×50 mL), water, and dried over magnesium sulfate. The solvent was concentrated in vacuo to yield a residue and purified by MPLC column chromatography (ethyl acetate/hexane, 3:7) to afford 5.63 g (65%) of 5-ethyl-2-[3-[2,6-dimethyl-4-(2-methyl-tetrazol-5-yl)phenoxy]propyl]furan (Formula II; R3 =5-ethyl, R4 =hydrogen, R1,R2 =3,5-dimethyl, R5 =2-methyltetrazol-5-yl, Y=1,3-propylene).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665763 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-5ab83aaac33e45579e689f23c6f4b675 |
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| Source note | uspto-grants-1997_09 |
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