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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255474Generated: October 26, 2026

Tetrahydrofuran → 3-Iodomethylcephem

https://huagongshe.com/reaction/255474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantN-methyl-N-(trimethylsilyl)trifluoroacetamideHCID 32510—
ReactantTrimethylsilyl iodideHCID 85247—
Reactant7beta-[2-(2-Aminothiazol-4-yl)-2-(4-chlorobenzyloxyimino)acetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acidHCID 131715275—
SolventDichloromethaneHCID 6344—
Product3-IodomethylcephemHCID 69068203—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a suspension of 200 mg (0.35 mmole) of 7β-[2-(2-aminothiazol-4-yl)-2-(4-chlorobenzyloxyimino)acetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid in 5 ml of methylene chloride was added 0.5 ml of MSTFA and the suspension was stirred at 40° C. until solution occurred. The solution was cooled to room temperature and 0.13 ml (0.87 mmole) of TMSI was added. The reaction stirred at room temperature for 30 minutes and evaporated to an oil. The oil was dissolved in 3 ml of acetonitrile and 0.12 ml (1.5 mmole) of THF was added. The mixture was then stirred at room temperature for 5 minutes to destroy excess TMSI and provide in solution the corresponding 3-iodomethyl-3-cephem derivative.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698338
Source datasetuspto-grants-1987_10
ORD IDord-a70f58c51dbe4e83bb5f58d4dea3b94d
Source noteuspto-grants-1987_10