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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456618Generated: November 1, 2026

Triphenylphosphine → HCID 22107118, compound

https://huagongshe.com/reaction/1456618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-HydroxyfluoreneHCID 75547—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantHCID 54262066HCID 54262066—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22107118HCID 2210711889.2%

Reaction Steps

A mixture of the compound prepared as described in Example 4 (0.462 g), triphenylphosphine (0.864 g), and 2-hydroxyfluorene (0.600 g) in tetrahydrofuran (4.2 ml) was cooled to approximately 1°-2° C., and treated with a solution of diethylazodicarboxylate (0.573 g) in tetrahydrofuran (1.7 ml) over a five minute period. After the addition was complete, the reaction was allowed to warm to room temperature. After about 24 hours, the resulting suspension was filtered, and the insolubles washed with tetrahydrofuran (5 ml) to give 0.526 g of methyl 3-(2-fluorenoxy)-2-pyrrolidone-5-carboxylate. This material was dried in a vacuum oven at 60° C. for approximately 24 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843997
Source datasetuspto-grants-1998_12
ORD IDord-435aa0f89c694a31bcecffb5642dcc06
Source noteuspto-grants-1998_12