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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591269Generated: October 31, 2026

Anisole → HCID 141560923, compound

https://huagongshe.com/reaction/1591269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 141560925HCID 141560925—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
SolventNitromethaneHCID 6375—
ProductHCID 141560923HCID 1415609237.7%

Reaction Steps

A solution of aluminum chloride (82 mg, 0.612 mmol) in nitromethane (1 mL) was added rapidly to a stirred, cooled (ice/H2O bath) solution of diphenylmethyl 7-[2-(2-aminothiazol-4-yl)-(Z)-2-methoxyiminoacetamido]-3-(2-benzyloxy-3,4-dioxo-1-cyclobutenyl)-3-cephem-4-carboxylate (50 mg, 0.068 mmol) and anisole (66 mg, 0.612 mmol) in CH2Cl2 (1 mL). The mixture was stirred with cooling for 0.33 hr and then for 2 hrs at ambient temperatures. The solution was cooled and diluted with dilute aqueous hydrochloric acid to precipitate a solid which was collected and discarded. The aqueous filtrate was washed with ethyl acetate. The aqueous layer was applied to a Michel-Miller HPLPLC column (22×130 mm) containing Partisil Prep 40 ODS-3. The column was eluted with a mixture of H2O-acetonitrile-acetic acid (90:10:0.5). The appropriate fractions were combined and the organic solvents removed. Lyophilization of the aqueous solution afforded the title compound (2.5 mg, 7.7 % yield) as a bright yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206360
Source datasetuspto-grants-1993_04
ORD IDord-bf266586278d46fc94939b824d42ff90
Source noteuspto-grants-1993_04