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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186044Generated: November 1, 2026

Triphenylphosphine → HCID 58245725, compound

https://huagongshe.com/reaction/1186044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4,5-dihydroxyphthalonitrileHCID 643390—
Reactant2-(2,2-Diethoxyethyl)-1,3-propanediolHCID 12200648—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58245725HCID 58245725—

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673890B2
Source datasetuspto-grants-2014_03
ORD IDord-40a97a138e47490d8eeb1641c3a8d7f1
Source noteuspto-grants-2014_03