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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514829Generated: October 25, 2026

2-Fluoro-6-nitroaniline → 2-Fluoro-6-nitrophenylthiocyanate

https://huagongshe.com/reaction/514829

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-6-nitroanilineHCID 87316—
ReactantPotassium thiocyanateHCID 516872—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product2-Fluoro-6-nitrophenylthiocyanateHCID 9041902299.9%

Reaction Conditions

Temperature5 °C

Reaction Steps

A solution of 2-fluoro-6-nitroaniline (3 g, 0.02 mol) in conc. sulphuric acid (30 mL) and water (30 mL) was diazotized at 0-3° C. for 90 min with aqueous sodium nitrite (1.45 g, 0.021 mol). After addition of potassium thiocyanate (2.522 g, 0.026 mol) in water (10 mL), the diazo-liquor was stirred vigorously into a suspension of cuprous thiocyanate (6.05 g, 0.05 mol) in water (20 mL) at 5° C. After stirring at 5° C. for 2 hr, the mixture was then heated at 70° C. for 20 min, then was cooled overnight, filtered, and the cake extracted with EtOAc to get the crude product (3.96 g) which was used in the next step without further purification. LC-MS: m/z 199.2 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108921B2
Source datasetuspto-grants-2015_08
ORD IDord-522fe75e085945588571e3fc32547aab
Source noteuspto-grants-2015_08