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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872298Generated: October 29, 2026

N-Methoxy-N-methyl-2-phenylacetamide → HCID 66665381, compound

https://huagongshe.com/reaction/872298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methyl-2-phenylacetamideHCID 10419762—
ReactantHCID 58229900HCID 58229900—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 66665381HCID 66665381—

Reaction Steps

A solution of 5-(4-bromo-phenyl)-2-oxa-4-aza-bicyclo[3.1.1]heptan-3-one (prepared according to WO2009/148916, 4 g) in dry THF (60 mL) was cooled to −78° C. and treated with n-BuLi (6.56 mL of a 2.5M solution in hexane) and stirred for 30 minutes at this temperature before addition of further n-BuLi (13.1 mL of a 2.5M solution in hexane). Stirring was continued at this temperature for 30 minutes before a solution of N-methoxy-N-methyl-benzeneacetamide (prepared according to US6407119B1, 4.6 g) in THF (10 mL) was added. After 10 minutes the reaction was quenched with saturated aqueous ammonium chloride solution, extracted with EtOAc and the combined organic phases washed with brine, filtered and concentrated. The residue was triturated with hexane/EtOAc to give the title compound which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975265B2
Source datasetuspto-grants-2015_03
ORD IDord-390350192f2947f3b4acc0ccb2377f88
Source noteuspto-grants-2015_03