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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614541Generated: October 30, 2026

2,6-Dichlorophenol → 3,5-Dichloro-4-hydroxyphenyl thiocyanate

https://huagongshe.com/reaction/1614541

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorophenolHCID 6899—
ReactantAmmonium thiocyanateHCID 15666—
SolventMethanolHCID 887—
Product3,5-Dichloro-4-hydroxyphenyl thiocyanateHCID 1088942014.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

2,6-Dichlorophenol (100 g, 0.613 mole) and ammonium thiocyanate (102.73 g, 1.350 mole) were mixed in methanol and the solution cooled to 0° C. Chlorine gas was bubbled through the reaction, maintaining the temperature below 10° C. The solution turned a pale yellow color. The reaction was stirred for a total of 3 hours until acidic at which time ammonia gas was bubbled through the reaction mixture and the solution stirred for an addtional three hours 0° to 10° C. The reaction was poured into iced distilled water, and filtered, yielding approximately 20 g of yellow solid which was dried overnight in vacuo. The filtrate was extracted with ethyl ether and the extract dried over magnesium sulfate and solvent removed in vacuo to yield approximately 100 g of crude product. Following purification by silica chromatography, the material was taken up in 1 liter of toluene, charcoal added, filtered and recrystallized from hexane to yield 55.03 g of product as yellow solid, m.p. ca. 945°-97° C. The structure was confirmed by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198435
Source datasetuspto-grants-1993_03
ORD IDord-f31a97883e5c49d6be52810eb29f3d03
Source noteuspto-grants-1993_03