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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249535Generated: October 31, 2026

2-Fluoroaniline → 2-Fluoro-4-thiocyanatoaniline

https://huagongshe.com/reaction/1249535

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoroanilineHCID 9584—
ReactantBromineHCID 24408—
ReactantSodium BromideHCID 253881—
ReactantSodium thiocyanateHCID 516871—
ReactantSodium BicarbonateHCID 516892—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Fluoro-4-thiocyanatoanilineHCID 435636586%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 550 ml of methanol were added 111 g of 2-fluoroaniline and 240 g of sodium thiocyanate, and the mixture was cooled to 0° C. A cooled (0° C.) solution of 176 g of bromine in 500 ml of methanol saturated with sodium bromide was added dropwise to the mixture over the period of 1 hour 15 minutes under stirring. In the course of this, cooling was effected so that the internal temperature might be maintained at not more than 3° C. After the addition of bromine was completed, the reaction mixture was poured in 2 l of cold water, and 100 g of sodium hydrogencarbonate was added to make the mixture weakly alkaline. The crystals, which separated out, were recovered by filtration and washed with cold water to give 144.5 g of crude 2-fluoro-4-thiocyanatoaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04632938
Source datasetuspto-grants-1986_12
ORD IDord-33ac32cdde3242aa99e061e63a65735a
Source noteuspto-grants-1986_12