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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615769Generated: October 30, 2026

Acetamide, 2-(trimethylsilyl)- → HCID 131712017, compound

https://huagongshe.com/reaction/615769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamide, 2-(trimethylsilyl)-HCID 357676—
ReactantBistrimethylsilylacetamidHCID 11708267—
Reactant(6R)-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 12941984—
ReactantHCID 54300440HCID 54300440—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 131712017HCID 13171201772.2%

Reaction Steps

N,N-Dimethylformamide (0.579 g.), phosphoryl chloride (1.214 g.) and ethyl acetate (3 ml.) were treated in a conventional manner to give a Vilsmeier reagent and the reagent was added to ethyl acetate (7 ml.). To the solution was added 2-(2,3-dihydro-1,4-oxathiin-6-yl)-2-n-hexyloxyiminoacetic acid (syn isomer, 2.00 g.) under stirring to give an activated acid solution. On the other hand, 7-amino-3-cephem-4-carboxylic acid (1.46 g.), trimethylsilylacetamide (3.84 g.), bis(trimethylsilyl)acetamide (4.40 ml.) and ethyl acetate (24 ml.) were stirred to prepare a solution. To the solution was added all at once the activated acid solution at -10° C., and stirred at the same temperature for 1.5 hours. After adding water (30 ml.) and ethyl acetate (15 ml.) to the resultant solution, the solution was shaken sufficiently and the organic layer was separated. An aqueous solution of sodium bicarbonate (30 ml.) was added to the organic solution, shaken sufficiently and the aqueous layer was separated. The solution was adjusted to pH 2.0 with conc.hydrochloric acid and extracted with ethyl acetate (60 ml.). The extract was washed with water (20 ml.) twice, dried over magnesium sulfate and concentrated in vacuo. The residue was pulverized with diisopropyl ether (50 ml.) and the precipitates were collected by filtration to give 7-[2-(2,3-dihydro-1,4-oxathiin-6-yl)-2-n-hexyloxyiminoacetamido]-3-cephem-4-carboxylic acid (syn isomer, 2.40 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04500709
Source datasetuspto-grants-1985_02
ORD IDord-209258233e4044669fe4ef397eeb7501
Source noteuspto-grants-1985_02