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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275968Generated: October 31, 2026

Triphenylphosphine → HCID 9823905, compound

https://huagongshe.com/reaction/275968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantEthyl 2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 11791243—
Reactant2-(9H-Fluoren-9-ylidene)ethan-1-olHCID 23445830—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9823905HCID 9823905—

Reaction Steps

Diethyl azodicarboxylate (0.235 ml, 1.49 mmol) was added at 0° C. to a stirred solution of triphenylphosphine (0.392 g, 1.49 mmol) and 2-fluoren-9-ylidene-ethanol (0.208 g, 1.0 mmol) in dry THF (5 ml) and the mixture stirred for 5 min. A solution of ethyl 2-ethoxy-3-(4-hydroxy-phenyl)-propionate (0.356 g, 1.49 mmol) in dry THF (5 ml) was then added, the mixture allowed to warm to room temperature, and stirring continued for 72 h. The resulting mixture was treated with water (50 ml), and the products extracted into dichloromethane (3×20 ml). The extracts were combined, washed with brine, dried (Na2SO4) and evaporated to a yellow gum. This was then purified by column chromatography on silica gel (15% Et2O in petroleum eluent) to give ethyl 2-ethoxy-3-[4-(2-fluoren-9-ylidene-ethoxy)-phenyl]-propionate as a yellow gum; 0.28 g (60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353018B1
Source datasetuspto-grants-2002_03
ORD IDord-99aeab48e28b49fe8a60fe25ed205e02
Source noteuspto-grants-2002_03