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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929491Generated: October 31, 2026

Diazomethane → HCID 58155344, compound

https://huagongshe.com/reaction/1929491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 58155181HCID 58155181—
Reactant38225-32-0HCID 86651224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58155344HCID 58155344—

Reaction Conditions

Temperature-75 °C

Reaction Steps

A dried flask was charged under an argon atmosphere with a solution of (R)-5-(3-bromo-phenyl)-4-(4-methoxy-benzyl)-5-methyl-morpholin-3-one (600 mg, 1.5 mmol) in tetrahydrofuran (16 ml) which was cooled to −75° C. Lithium isopropylamine (1.54 ml, 3 mmol) was added, and after the addition of diazomethane (502 mg, 3.5 mmol) the reaction was complete. For the workup, the cold reaction mixture was quenched with a saturated ammonium chloride solution (15 ml) and extracted with a mixture of dichloromethane (40 ml) and water (15 ml). The organic layer was dried over sodium sulfate and evaporated to yield the crude (2S,5R)-5-(3-bromo-phenyl)-4-(4-methoxy-benzyl)-2,5-dimethyl-morpholin-3-one as a brownish oil which was engaged in the next step without further purification. Mass (calculated) C20H22BrNO3 [404.307]; (found) [M+H]+=404, [M+2-H]+=406.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188079B2
Source datasetuspto-grants-2012_05
ORD IDord-7832fbf9dc3d42a2854e08d10aad3b14
Source noteuspto-grants-2012_05