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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929490Generated: October 30, 2026

4-Methoxybenzyl bromide → HCID 58155181, compound

https://huagongshe.com/reaction/1929490

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl bromideHCID 165021—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 66931638HCID 66931638—
SolventDimethylformamideHCID 6228—
ProductHCID 58155181HCID 58155181—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (R)-5-(3-amino-phenyl)-4-(4-methoxy-benzyl)-5-methyl-morpholin-3-one (1.0 g, 3.7 mmol) in N,N-dimethylformamide was added within 5 minutes at 0° C. to a solution of potassium tert-butanolate (0.636 g, 5.7 mmol). After stirring at 0° C. for 30 minutes the light yellow solution was cooled to −4° C. and treated with a solution of 4-methoxybenzylbromide (1.12 g, 5.6 mmol) in N,N-dimethylformamide (4 ml). The reaction mixture was left to warm to room temperature, then the solvent was evaporated at reduced pressure, and the residue treated with saturated ammonium chloride solution (50 ml) and ethyl acetate (100 ml). The organic layer was separated, washed with brine (50 ml), dried over sodium sulfate, and evaporated at reduced pressure. The crude product was purified by chromatography on silica gel using a gradient of heptane and ethyl acetate=100/0 to 50/50 as the eluent. The (R)-5-(3-bromo-phenyl)-4-(4-methoxy-benzyl)-5-methyl-morpholin-3-one was obtained as colorless oil (1.19 g, 83% of theory). Mass (calculated) C19H20BrNO3 [390.275]; (found) [M+H]+=390, [M+2-H]+=392.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188079B2
Source datasetuspto-grants-2012_05
ORD IDord-df916bd456fe46e29356ad28103a1908
Source noteuspto-grants-2012_05