HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186044Generated: November 1, 2026
Triphenylphosphine → HCID 58245725, compound
https://huagongshe.com/reaction/1186044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 4,5-dihydroxyphthalonitrile | HCID 643390 | — |
| Reactant | 2-(2,2-Diethoxyethyl)-1,3-propanediol | HCID 12200648 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58245725 | HCID 58245725 | — |
Reaction Steps
To the mixture of 4,5-dihydroxy-phthalonitrile (2.50 g, 15.6 mmol), 2-(2,2-diethoxy-ethyl)-propane-1,3-diol (4.5 g, 23.4 mmol) and triphenylphosphine (6.138 g, 23.4 mmol) in THF (40 mL) was added diethyl azodicarboxylate (4.08 g, 23.4 mmol) and the resulting mixture heated at 75° C. overnight. The resulting mixture was then cooled to room temperature and evaporated in vacuo to yield a solid, which was purified via flash column chromatography (EA/Hex 2:3) to yield 3-(2,2-diethoxyethyl)-3,4-dihydro-2H-benzo[b][1,4]dioxepine-7,8-dicarbonitrile as a white solid. MS MH+=317, 1H NMR (CDCl3) δ 7.29 (s, 2H), 4.58 (m, 1H), 4.46 (m, 2H), 4.19 (m, 2H), 3.66 (m, 2H), 3.52 (m, 2H), 2.60 (m, 1H), 1.78 (m, 2H), 1.20 (t, J=7.0 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673890B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-40a97a138e47490d8eeb1641c3a8d7f1 |
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| Source note | uspto-grants-2014_03 |
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