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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484037Generated: October 30, 2026

Phenylacetyl chloride → HCID 14543802, compound

https://huagongshe.com/reaction/484037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantP-AnisidineHCID 7732—
ReactantEthyl oxoacetateHCID 70211—
ReactantHCID 20086945HCID 20086945—
Solvent1,2-DichloroethaneHCID 11—
Solvent1,1-DichloroethaneHCID 6365—
SolventTriethylamineHCID 8471—
ProductHCID 14543802HCID 14543802—

Reaction Steps

To a solution of 17 ml of triethylamine and 5.0 g of the imine formed from ethyl glyoxalate and p-anisidine in 100 ml of refluxing 1,2-dichloroethane was added dropwise over 2 hours a solution of 16 ml of freshly distilled phenylacetyl chloride in 50 ml of dichloroethane. After refluxing for three hours the reaction was worked-up as per the 3-azidoazetidinone. The crude residue was chromatographed to yield the cis and trans isomers of 4-carboethoxy-1-(p-methoxyphenyl)-3-phenylazetidin-2-one as oils; cis: NMR (CDCl3): δ 7.2 (m, 7H), 6.7 (d, J=9, 2H), 4.7 (s, 2H), 3.6 (s, 3H), 3.6 (q, J=7, 2H), 0.7 (t, J=7, 3H); trans: NMR (CDCl3): δ 7.3 (m, 7H), 6.8 (d, J=9, 2H), 4.5 (d, J=2, 1H), 4.45 (d, J=2, 1H), 4.1 (q, J=7, 2H), 3.6 (s, 3H), 1.2 (t, J=7, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05229381
Source datasetuspto-grants-1993_07
ORD IDord-29fd0eca41774ab8a1f0e04c420c4f67
Source noteuspto-grants-1993_07