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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253327Generated: October 31, 2026

Hydrochloric Acid → HCID 66842008, compound

https://huagongshe.com/reaction/253327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantStannous chloride dihydrateHCID 61436—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 66777200HCID 66777200—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
ProductHCID 66842008HCID 6684200891.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

53 g of sodium nitrite was added to 300 ml of concentrated sulfuric acid at 50° C. or lower, and 300 ml of acetic acid was added dropwise at 50° C. or lower. To this mixed solution, 100 ml of an acetic acid solution of 182 g of 2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)aniline was added dropwise over a period of 2 hours at 20° C. or lower, followed by stirring at 20° C. for 3 hours. The reaction mixture was added dropwise at 5° C. or lower to a mixed solution of 390 g of tin(II)chloride dihydrate and 1,000 ml of 6N hydrochloric acid, followed by stirring for 30 minutes. Toluene was added to this reaction mixture, and the reaction mixture was neutralized with a 10% aqueous sodium hydroxide solution. The insolubles were filtered off, and the organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 177 g of 2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenylhydrazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872036B2
Source datasetuspto-grants-2011_01
ORD IDord-c1bacade75ac4875818fa8624f58cc6a
Source noteuspto-grants-2011_01