HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993367Generated: October 31, 2026
Triphenylphosphine → HCID 21876847, compound
https://huagongshe.com/reaction/993367
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Tetrahydro-4H-pyran-4-ol | HCID 74956 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 4-Hydroxy-4'-nitrobenzophenone | HCID 11096817 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21876847 | HCID 21876847 | 61.1% |
Reaction Steps
Diethyl azodicarboxylate (1.47 g, 8.4 mmol) was slowly added dropwise to a solution of 4-(4-hydroxybenzoyl)-nitrobenzene (1.7 g, 7mmol) (prepared as described in Example 1, steps), 4-hydroxytetrahydropyran (0,78 g, 7.7 mmol) and triphenylphosphine (2.2 g, 8.4mmol) in dry tetrahydrofuran (20 mL) while stirring at room temperature under inert atmosphere. The reaction mixture was stirred for an additional hour then quenched with water (1 mL) and concentrated in vacuo. The residue was diluted with water and extracted with ethyl acetate The combined organic extracts were washed with water and brine, dried (Na2SO4), and concentrated in vacuo. The crude product was chromatographed on silica gel (25% ethyl acetate/hexanes) and crystallized from hexanes to give 4-(4-tetrahydropyran-4-yloxybenzoyl)-nitrobenzene (1.4 g, 61%) as a white solid, m.p. 105-106 ° C.; Analysis for C18H17NO5: Calc.: C, 66.05; H, 5.23; N, 4.28; Found: C, 65.95; H, 3.14; N, 4.38. MS m/e (%): 283 (M+; 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472536B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-70b3195a97b8420b9efb0b8085677d64 |
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| Source note | uspto-grants-2002_10 |
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