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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073837Generated: October 31, 2026

Thionyl Chloride → HCID 23364532, compound

https://huagongshe.com/reaction/2073837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23364529HCID 23364529—
SolventChloroformHCID 6212—
ProductHCID 23364532HCID 2336453247.9%

Reaction Steps

A solution of 5.81 g (18.4 mmol) of N-(2-hydroxy-1,1-dimethylethyl)-2,4,5-trifluoro-3-(trifluoromethyl)-benzamide in 100 ml of chloroform at 0° C. was treated dropwise with 5 ml of thionyl chloride. The mixture was allowed to warm to room temperature overnight. The solution was concentrated to a yellow oil which was dissolved in 20 ml of DMF and treated with 0.8 g (21.6 mmol) of 60% sodium hydride. This reaction mixture was stirred at room temperature for 18 hours, then poured into 50 ml of dilute NaHCO3. The solution eas extracted with ethyl acetate; the organic phase was washed with water and dried over magnesium sulfate. Concentration in vacuo gave an orange oil which was chromatographed on silica, eluting with 2% methanol in chloroform, to give 2.62 g of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920120
Source datasetuspto-grants-1990_04
ORD IDord-000777943dcd482cb5d42161b9615c5a
Source noteuspto-grants-1990_04