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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947285Generated: October 26, 2026

Hydrochloric Acid → Methyl 3-bromo-4-hydroxy-5-(3-morpholino-3-oxopropanoyl)benzoate

https://huagongshe.com/reaction/1947285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Morpholinecarbonyl chlorideHCID 84810—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantMethyl 3-acetyl-5-bromo-4-hydroxybenzoateHCID 15818980—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-bromo-4-hydroxy-5-(3-morpholino-3-oxopropanoyl)benzoateHCID 5823504090.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of lithium bis(trimethylsilyl)amide (1.41 L, 1406 mmol) at −65° C. under nitrogen was added dropwise methyl 3-acetyl-5-bromo-4-hydroxybenzoate (120 g, 439 mmol) in THF (1.2 L). The solution was allowed to warm to 0° C., and maintained at this temperature for 1 hr. The solution was cooled back to −65° C. and morpholine-4-carbonyl chloride (0.055 L, 483 mmol) was added. The mixture was stirred at RT for 2 hrs then cooled to −30° C., DCM (1.5 L) and water (1 L) were added followed by dropwise addition of HCl 6N (500 mL) then HCl2N (300 mL) until pH 7, the aqueous solution was extracted with DCM (3×). The combined extracts were dried over magnesium sulfate and evaporated. The crude product was triturated in MTBE to obtain methyl 3-bromo-4-hydroxy-5-(3-morpholino-3-oxopropanoyl)benzoate (153 g, 90%) as a beige solid. Mass Spectrum: M+H+ 388.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399460B2
Source datasetuspto-grants-2013_03
ORD IDord-8b5804a26d72434cb6089739ad9233c7
Source noteuspto-grants-2013_03