HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247688Generated: October 26, 2026
Triphenylphosphine → {4-[3,3-Bis-(2-furanyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester
https://huagongshe.com/reaction/1247688
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 3,3-Bis-(2-furanyl)-prop-2-en-1-ol | HCID 21907760 | — |
| Reactant | Ethyl [4-sulfanyl-2-(trifluoromethyl)phenoxy]acetate | HCID 59516001 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {4-[3,3-Bis-(2-furanyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester | HCID 68577859 | — |
Reaction Steps
To a solution of 3,3-bis-(2-furanyl)-prop-2-en-1-ol (104 mg, 0.55 mmol) and triphenylphosphine (275 mg, 1.09 mmol) in THF (10 ml) was added, at room temperature and under nitrogen atmosphere, DEAD (190 mg, 1.09 mmol). The reaction mixture was stirred for 5 min after which (2-trifluoromethyl4-mercapto-phenoxy)-acetic acid ethyl ester (230 mg, 0.82 mmol) was added over 15 min. The reaction mixture was stirred at 0oC for 2 hours followed by 18 hours at room temperature and 3 hours at 50° C. The reaction mixture was evaporated and the crude residue was purified on column chromatography using ethyl acetate as eluent. The desired {4-[3,3-bis-(2-furanyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester was isolated in 11 mg yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129268B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-f424a99be8ed4ead94c7c10705857c11 |
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| Source note | uspto-grants-2006_10 |
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