HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035713Generated: October 29, 2026
Triphenylphosphine → HCID 178501274, compound
https://huagongshe.com/reaction/1035713
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 178501285 | HCID 178501285 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178501274 | HCID 178501274 | 71.4% |
Reaction Steps
1.1 g of methyl trans-4-hydroxycyclohexanecarboxylate (6.95 mmol, 1.35 eq.), 1 g of tert-butyl 4-hydroxybenzoate (5.15 mmol, 1 eq.) and 2.03 g of triphenylphosphine (7.72 mmol, 1.5 eq.) are placed in 10 mL of tetrahydrofuran at room temperature. 1.5 mL of diisopropyl azodicarboxylate (7.72 mmol, 1.5 eq.) are added dropwise to the reaction medium with stirring. After 18 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 with sodium hydroxide solution, 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 0% to 50%. 1.23 g of tert-butyl cis-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-03ce3ce052bb48d5b64f36674652cc40 |
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| Source note | uspto-grants-2013_10 |
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