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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856989Generated: October 25, 2026

4-Morpholinecarbonyl chloride → (6-Fluoro-2,2-diphenyl-benzo[1,3]dioxol-5-yl)-morpholin-4-yl-methanone

https://huagongshe.com/reaction/856989

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Morpholinecarbonyl chlorideHCID 84810—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromo-6-fluoro-2,2-diphenyl-2H-1,3-benzodioxoleHCID 21865386—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product(6-Fluoro-2,2-diphenyl-benzo[1,3]dioxol-5-yl)-morpholin-4-yl-methanoneHCID 1002423668%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a cooled (−78° C.) solution of 5-bromo-6-fluoro-2,2-diphenyl-benzo[1,3]dioxole (17.59 g, 47.4 mmol) in diethyl ether (300 ml) was slowly added a solution of n-butyl lithium in hexanes (1.6M, 30 ml, 48 mmol, 1.0 eq.). The reaction mixture was stirred 1 h at −78° C. before the addition of 4-morpholinecarbonylchloride (8.5 g, 56.9 mmol, 1.2 eq.). The reaction mixture was allowed to warm to 20° C. and poured into an aqueous solution of sodium bicarbonate. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine. Volatiles were removed in vacuo. Purification by flash chromatography afforded (6-fluoro-2,2-diphenyl-benzo[1,3]dioxol-5-yl)-morpholin-4-yl-methanone compound (13.0 g, 68%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144890B2
Source datasetuspto-grants-2006_12
ORD IDord-dc303e1cc50343c3afbc0eee43a6ca36
Source noteuspto-grants-2006_12