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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484681Generated: October 25, 2026

2,6-Dimethoxybenzoyl chloride → (3S-trans)-3-[(2,6-dimethoxybenzoyl)amino]-4-methyl-1-[(phenylmethyl)oxy]-2-azetidinone

https://huagongshe.com/reaction/484681

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dimethoxybenzoyl chlorideHCID 74810—
ReactantToluenesulfonateHCID 3424274—
Reactant(3S-trans)-3-amino-4-methyl-1-(phenylmethoxy)-2-azetidinoneHCID 13036842—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(3S-trans)-3-[(2,6-dimethoxybenzoyl)amino]-4-methyl-1-[(phenylmethyl)oxy]-2-azetidinoneHCID 13036849—

Reaction Steps

To a cold (-10° C.) solution of (3S-trans)-3-amino-4-methyl-1-(phenylmethoxy)-2-azetidinone, toluenesulfonate (0.95 g; see example 2D) in methylene chloride (50 ml) is added 2,6-dimethoxybenzoyl chloride (0.60 g) and 4-dimethylaminopyridine (0.61 g). The reaction is stirred under nitrogen and allowed to rise to 26° C. over five hours. The reaction mixture is concentrated to an oil and partitioned between ethyl acetate and aqueous hydrogen sulfate solution. The organic layer is washed with aqueous sodium bicarbonate, and brine, dried over sodium sulfate and concentrated to a foam (0.848 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04533660
Source datasetuspto-grants-1985_08
ORD IDord-b3c4aefaa8124d5eaa3567e0899a03f9
Source noteuspto-grants-1985_08