HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035695Generated: November 1, 2026
Triphenylphosphine → HCID 178501275, compound
https://huagongshe.com/reaction/1035695
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | tert-Butyl 4-hydroxybenzoate | HCID 117640 | — |
| Reactant | HCID 178501284 | HCID 178501284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178501275 | HCID 178501275 | 34.5% |
Reaction Steps
2.20 g of methyl cis-4-hydroxycyclohexanecarboxylate (13.88 mmol, 1 eq.), 2.70 g of tert-butyl 4-hydroxybenzoate (13.88 mmol, 1 eq.) and 5.46 g of triphenylphosphine (20.82 mmol, 1.5 eq.) are placed in 30 mL of tetrahydrofuran at room temperature. 4.04 mL of diisopropyl azodicarboxylate (20.82 mmol, 1.5 eq.) are added dropwise to the reaction medium with stirring. After 3 hours at room temperature, the medium is concentrated to dryness and taken up in diethyl ether. The triphenylphosphine oxide is filtered off. The organic phase is washed successively with sodium hydroxide solution and then with water, dried over sodium sulfate, filtered and evaporated to give a residue. This residue is chromatographed on silica gel, eluting with a gradient of ethyl acetate in heptane ranging from 10% to 50%. 1.6 g of tert-butyl trans-4-(4-methoxycarbonylcyclohexyloxy)benzoate are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546391B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-941cbb9b38ed4933a067b274588cc97c |
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| Source note | uspto-grants-2013_10 |
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