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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689320Generated: October 30, 2026

N-Formylmorpholine → HCID 76698013, compound

https://huagongshe.com/reaction/1689320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FormylmorpholineHCID 20417—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-1-fluoro-2-(2-methoxyvinyl)benzeneHCID 66973965—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418918HCID 178418918—
Solvent2-MethyltetrahydrofuranHCID 7301—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 76698013HCID 76698013—

Reaction Conditions

Temperature-10 °C

Reaction Steps

4-Bromo-1-fluoro-2-(2-methoxyvinyl)benzene (limiting reagent) (step c) was dissolved in 2-methyltetrahydrofuran (5 volumes) and the solution cooled to −10° C. Iso-propylmagnesium chloride (0.37 molar equivalents of a 2M solution in THF) was added dropwise, keeping the temperature at −7° C. (+ or −2° C.), over about 30 minutes, followed by Butyllithium (0.74 molar equivalents of a 1.5M solution in hexane), controlling the temperature at −6° C. (+ or −2° C.), over about 1 hour. Stirred for 45 minutes then added to a solution of 4-formylmorpholine (2 molar equivalents) in 2-methyltetrahydrofuran (7 volumes) at −5° C. This addition took about 90 minutes. The reaction was then stirred for 1 hour, during which time the internal temperature rose to 5° C. The reaction mixture was poured into saturated aq. ammonium chloride solution (10 volumes) and extracted with t-BME (2×3 volumes). Combined extracts were washed with sat'd aq. ammonium chloride (until the pH of the washing was approx 6) (2×3 volumes), water (5 volumes), dried (Na2SO4), filtered and evaporated to give a mobile orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-6099e6d0dedc4a3d9e4a08436a7e3eeb
Source noteuspto-grants-2012_04