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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296578Generated: October 31, 2026

Sodium Iodide → HCID 70507474, compound

https://huagongshe.com/reaction/2296578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
ReactantChloromethyl pivalateHCID 87885—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 70508451HCID 70508451—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 70507474HCID 70507474—

Reaction Steps

3-Methyl-7-(5-methyl-3-phenylisoxazole-4-carboxamido)ceph-3-em-4-carboxylic acid (25.9 g., 65 mmoles) was dissolved in anhydrous dimethylformamide (150 ml.). Triethylamine (19.7 g., 195 mmoles), potassium bicarbonate (19.5 g., 195 mmoles), sodium iodide (29.3 g., 195 mmoles) and chloromethyl pivalate (29.3 g., 195 mmoles) were added. An exotherm was noted, the temperature rising to approximately 35° C. After stirring for 6 hours at ambient temperature, monitoring by tlc (4:1 chloroform:ethyl acetate) indicated considerable starting material remained. Additional chloromethyl pivalate (8.4 g., 65 mmoles) was added and stirring at ambient temperature continued for 16 hours. Isolation as detailed in Preparation 1 gave pivaloyloxymethyl 3-methyl-7-(5-methyl-3-phenylisoxazole-4-carboxamido)ceph-3-em-4-carboxylate [25.3 g., 76%; Rf 0.8 (4:1 chloroform:ethyl acetate; ir (CH2Cl2) 1780, 1750, 1670 cm-1 ].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04429128
Source datasetuspto-grants-1984_01
ORD IDord-6481d26e83e3479c97d3ae3d8e03e226
Source noteuspto-grants-1984_01