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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479624Generated: October 26, 2026

Ammonium thiocyanate → 2,3,6-Trimethyl-4-thiocyanato-phenol

https://huagongshe.com/reaction/479624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium thiocyanateHCID 15666—
Reactant2,3,6-TrimethylphenolHCID 17016—
SolventMethanolHCID 887—
Product2,3,6-Trimethyl-4-thiocyanato-phenolHCID 2350381897%

Reaction Conditions

Temperature0 °C

Reaction Steps

2,3,6-trimethylphenol (1.6 g, 11.8 mmol) was disolved in 50 mL of anhydrous methanol which had been deoxygenated by bubbling with nitrogen. Ammonium thiocyanate (2.2 g, 28,9 mmol) was added to this solution which was then cooled to 0° C. and bubbled with chlorine gas. The initially colorless homogeneous solution becomes pink and then green with the formation of a white precipitate. The solution was stirred for 1 h at 0° C. and then for a further hour at 20° C. The dissolved chlorine was removed by bubbling with nitrogen and the precipitate removed by filtration. Evaporation of the filtrate under reduced pressure followed by drying under high vacuum (0.1 torr) yielded 2.20 g (97%) of 2,3,5-Trimethyl-4-hydroxyphenylthiocyanate in a form pure enough for the next step in the synthesis. An analytical sample was recrystallized from hexanes:white crystals, mp 100.3° C. 1H NMR (CDCl3) δ7.2 (s, 1H), 5.0 (s, 1H) 2.4 (s, 3H), 2.2 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645998B2
Source datasetuspto-grants-2003_11
ORD IDord-71c151efd1b24424b26ec9e481120abf
Source noteuspto-grants-2003_11