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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435735Generated: October 25, 2026

Salicyloyl chloride → HCID 178513857, compound

https://huagongshe.com/reaction/435735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicyloyl chlorideHCID 74041—
ReactantHCID 178514233HCID 178514233—
SolventAcetonitrileHCID 6342—
ProductHCID 178513857HCID 178513857—

Reaction Steps

A 25 ml. portion of dry acetonitrile is added to a mixture of 1.3 g. of the s-triazole carboxamide sodium salt and 2 g. of salicyloyl chloride followed by a few pellets of 4A molecular sieves. The mixture is stirred at room temperature for 16 hours and then filtered through Celite. The colorless solid is obtained on evaporating the filtrate is washed with diethyl ether; yield, 1 g., m.p. 147°-150° C. (dec.). Its infrared spectrum is essentially the same as that obtained from the product in Example 7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006159
Source datasetuspto-grants-1977_02
ORD IDord-fc5a8c5d9c524162bb776eeae08319f4
Source noteuspto-grants-1977_02