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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253239Generated: October 30, 2026

N-methyl-N-(trimethylsilyl)trifluoroacetamide → HCID 14030499, compound

https://huagongshe.com/reaction/1253239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-N-(trimethylsilyl)trifluoroacetamideHCID 32510—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 13326764HCID 13326764—
SolventDichloromethaneHCID 6344—
ProductHCID 14030499HCID 14030499—

Reaction Steps

7β-[(Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid (486 mg) was suspended in methylene chloride (9 ml), followed by an addition of N-methyl-N-(trimethylsilyl)trifluoroacetamide (980 μl). The resulting mixture was stirred at room temperature for 1 hour. After ice-cooling, iodotrimethylsilane (410 μl) was added and the resulting mixture was stirred for 15 minutes. The reaction mixture was concentrated under reduced pressure to obtain the silylated derivative of 7β-[(Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetamido]-3-iodomethyl-3-cephem-4-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04748171
Source datasetuspto-grants-1988_05
ORD IDord-14393c7ee83841669950709502729ac5
Source noteuspto-grants-1988_05