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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197122Generated: November 2, 2026

Oxalyl chloride → HCID 86745860, compound

https://huagongshe.com/reaction/1197122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67899853HCID 67899853—
SolventDichloromethaneHCID 6344—
ProductHCID 86745860HCID 86745860100%

Reaction Steps

3.5 g (0.01 mol) of 8-carboxy-6-(2-chlorophenyl)-1-methyl[1,2,4]triazolo-[4,3-a][1,4]benzodiazepine are suspended in 40 ml of dichloromethane. While cooling in ice, 2.5 g (0.02 mol) of oxalyl chloride are added dropwise, and the mixture is stirred at room temperature for 2 hours. It is then concentrated and subsequently distilled twice with anhydrous chloroform. The crystalline residue is triturated with petroleum ether and filtered off with suction. 3.7 g (100%) of 8-chlorocarbonyl-6-(2-chlorophenyl)-1-methyl[1,2,4]- triazolo[4,3-a][1,4]benzodiazepine of melting point 295°-297° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116971
Source datasetuspto-grants-1992_05
ORD IDord-e9cc866da5654f22a17be52f26d205b4
Source noteuspto-grants-1992_05