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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356500Generated: October 25, 2026

Bromine → 5-tert-Butyl-2-methyl-4-thiocyanato-phenol

https://huagongshe.com/reaction/356500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant5-tert-Butyl-o-cresolHCID 79845—
ReactantSodium BromideHCID 253881—
ReactantCID 86753328HCID 86753328—
SolventMethanolHCID 887—
Product5-tert-Butyl-2-methyl-4-thiocyanato-phenolHCID 10560955—

Reaction Conditions

Temperature40 °C

Reaction Steps

In a 5 L flask were placed 350 g (2.13 mol) of 5-tert-butyl-2-methyl-phenol, sodium thiocyanide (555 g, 6.85 mol) and MeOH (1400 mL), and the resulting mixture cooled to 7° C. A solution of sodium bromide (214 g, 2.08 mol), bromine (126 mL, 2.38 mol), and MeOH (1800 mL) was added slowly and the temperature raised to 40° C. over a period of 30 minutes. The precipitants were filtered and the filtrate concentrated by half. Saturated sodium carbonate (3.5 L) and H2O (4.5 L) were added. The mixture was extracted with EtOAc (3 L), and the organic layers were combined and concentrated. To this residue were added t-butylmethyl ether (500 mL) and hexanes (500 mL), and the mixture was allowed to stand for 17 hours at -5° C. The precipitants were filtered to give the title compound, m.p. 99°-102° C. 1H NMR (CDCl3) δ 1.46 (s, 9 H), 2.22 (s, 3 H), 5.01 (s, 1 H), 6.89 (s, 1 H), 7.49 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834506
Source datasetuspto-grants-1998_11
ORD IDord-aefea9b903b04ba99103150098733d61
Source noteuspto-grants-1998_11