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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131138Generated: November 1, 2026

Water → HCID 22064029, compound

https://huagongshe.com/reaction/131138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
Reactant4-(4-Bromo-3-methoxyphenyl)morpholineHCID 22064039—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22064029HCID 2206402966%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 4-bromo-3-methoxy-1-morpholinobenzene (104 mg, 0.382 mmol) in anhydrous tetrahydrofuran (3 mL) at −78° C. was slowly added n-butyl lithium (1.3 M solution in hexanes, 325 μL, 0.420 mmol) under nitrogen. The cooling medium was exchanged with an ice-bath, and the mixture was stirred for 5 min. After cooling again to −78° C., carbon dioxide from evaporation of dry ice was bubbled through the solution for 10 min. A precipitate was formed, and the reaction mixture was allowed to reach room temperature. Diethyl ether and water were added. The mixture was extracted, the layers were separated, and the aqueous layer was acidified to pH 4. The dark blue aqueous solution was extracted several times with diethyl ether and ethyl acetate at pH 4 to pH 6. The combined organic layers were dried (MgSO4), and the solvent was removed in vacuo affording 60 mg (66% yield) of the title compound as a white solid: mp 158-160° C.; EIMS m/z (relative intensity) 237 (100, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384943B2
Source datasetuspto-grants-2008_06
ORD IDord-ebe9f48ca0a24c5bb3346a94a58c6f38
Source noteuspto-grants-2008_06