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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085413Generated: October 28, 2026

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

https://huagongshe.com/reaction/1085413

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 and the solution stirred for an additional three hours at 0° to 10° C. The reaction was poured into iced distilled water, and filtered, yielding approximately 20 g of a yellow solid which was dried overnight in vacuo. The filtrate was extracted with ethyl acetate, the extracts dried over magnesium sulfate and solvent removed in vacu 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 a yellow solid, m.p. about 94.5°-97° C. The structure was confirmed by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05010080
Source datasetuspto-grants-1991_04
ORD IDord-86ac73f329da43c09c1b6ee6736718df
Source noteuspto-grants-1991_04