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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828769Generated: November 1, 2026

Phosgene → 5-(9H-fluoren-9-ylmethoxy)-3H-1,3,4-oxadiazol-2-one

https://huagongshe.com/reaction/1828769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
Reactant9-Fluorenylmethyl carbazateHCID 161883—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-(9H-fluoren-9-ylmethoxy)-3H-1,3,4-oxadiazol-2-oneHCID 1075517683%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of N-[(9H-fluoren-9-ylmethoxy)carbonyl]hydrazine (141) (1.49 g, 5.78 mmol), CH2Cl2 (60 ml) and saturated NaHCO3 solution (60 ml) was stirred vigorously at 0° C. for 5 minutes, and the solution was then left for 5 minutes without stirring. Phosgene (1.89 M in toluene, 7.95 ml, 15.0 mmol) was then carefully added to the lower, organic phase using a syringe, and stirring of the reaction mixture was begun again immediately after the addition. After 10 minutes, water (20 ml) and CH2Cl2 (20 ml) were added to the reaction mixture. The phases were then separated rapidly, the aqueous phase was extracted with CH2Cl2 (50 ml), and the combined organic phases were dried over Na2SO4. Removal of the solvent under reduced pressure and drying gave a colourless solid (1.35 g, 4.82 mmol, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060707B2
Source datasetuspto-grants-2006_06
ORD IDord-726240ce1d7c4e2f8de4cc0882c90c2a
Source noteuspto-grants-2006_06