Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183222Generated: November 2, 2026

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

https://huagongshe.com/reaction/1183222

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 dissolved 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) δ 7.2 (s, 1H), 5.0 (s, 1H) 2.4 (s, 3H), 2.2 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664264B2
Source datasetuspto-grants-2014_03
ORD IDord-5bb5df7056e84884a17a0a20b219c222
Source noteuspto-grants-2014_03