HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015368Generated: October 31, 2026
Triphenylphosphine → HCID 67302000, compound
https://huagongshe.com/reaction/1015368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ethyl 4-hydroxycyclohexanecarboxylate | HCID 86973 | — |
| Reactant | 2,6-Difluorophenol | HCID 94392 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67302000 | HCID 67302000 | 34% |
Reaction Steps
4-Hydroxycyclohexanecarboxylic acid ethyl ester (300 mg; 1.7 mmol), triphenylphosphine (1 g; 4.2 mmol) and 2,6-difluorophenol (340 mg; 2.6 mmol) were stirred in anhydrous toluene and chilled to 0° C. under nitrogen flow. Diethyl azodicarboxylate (2 mL; 4.3 mmol) was added to the mixture over 1 minute and warmed to room temperature. Reaction continued for 16 hours. Reaction was quenched with water, and mixture was extracted with 4×5 mL with ethyl acetate. Combined organics were washed with brine and dried over MgSO4. Oily residue was triturated with diethyl ether and solids filtered off. Filtrate was concentrated at reduced pressure and purified via flash chromatography using 5-20% ethyl acetate in hexanes to give 162 mg of title compound. (34% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985755B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-eda9ecee2a4f4c428c61ec6e30987edd |
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| Source note | uspto-grants-2011_07 |
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