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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979900Generated: October 31, 2026

Chlorotrimethylsilane → (2S,3S)-3-Amino-2-methyl-4-oxo-1-azetidinesulfonic acid

https://huagongshe.com/reaction/1979900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant(3S-trans)-4-methyl-2-oxo-3-(phenyloxycarbonylamino)-1-azetidinesulfonic acid, tetrabutylammonium saltHCID 131713967—
Solvent1,2-DichloroethaneHCID 11—
Product(2S,3S)-3-Amino-2-methyl-4-oxo-1-azetidinesulfonic acidHCID 13336165.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 531 mg (0.001 mole) of (3S-trans)-4-methyl-2-oxo-3-(phenyloxycarbonylamino)-1-azetidinesulfonic acid, tetrabutylammonium salt in 10 ml of 1,2-dichloroethane is treated with 278 μl of triethylamine and 250 μl of trimethyl chlorosilane and the solution refluxed for 75 minutes. An aliquot of the reaction mixture shows intense IR absorption of 2270 cm-1 (indicative of the isocyanate group) and almost complete disappearance of the 1745 cm-1 band (for the urethane function) in addition to a strong absorption at 1770 cm-1 (β-lactam). The solution is refluxed for 20 hours (no change in IR), cooled to 0° C., and 2 ml of 88% formic acid is added. After 2.5 hours at room temperature the slurry is filtered to give 118 mg of (3S-trans)-3-amino-4-methyl-2-oxo-1-azetidinesulfonic acid, inner salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04483797
Source datasetuspto-grants-1984_11
ORD IDord-f8a62bf236cb4edebc3499d6670246bb
Source noteuspto-grants-1984_11