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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867592Generated: October 30, 2026

Oxalyl chloride → HCID 178465412, compound

https://huagongshe.com/reaction/867592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178465411HCID 178465411—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 178465412HCID 178465412—

Reaction Steps

1-(o-nitrobenzyloxycarbonyltriphenylphosphoranylmethyl)-3-(1-o-nitrobenzyloxycarbonylaminoethyl)-4-(carboxymethyl)-2-azetidinone (0.1320 g from the previous step) is dissolved in 5 ml CH2Cl2 and cooled to 0° under N2. Oxalyl chloride (0.040 ml, 0.44 mmole) is added dropwise over 5 minutes and then 1 drop of DMF is added. The mixture is stirred at 0° for 5 minutes and then at 25° C. for another 15 minutes. The solvent and excess oxalyl chloride are evaporated under reduced pressure. The residue is then desired acid chloride which is used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775669
Source datasetuspto-grants-1988_10
ORD IDord-4870b7c336c14dd9a815ada757ae8356
Source noteuspto-grants-1988_10