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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254642Generated: October 26, 2026

Bromine → 4-Methyl-6-trifluoromethoxy-2-benzothiazolamine

https://huagongshe.com/reaction/2254642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
Reactant2-Methyl-4-(trifluoromethoxy)anilineHCID 2775546—
SolventAcetic AcidHCID 176—
SolventCyclohexaneHCID 8078—
Product4-Methyl-6-trifluoromethoxy-2-benzothiazolamineHCID 1467448171.1%

Reaction Steps

The procedure is as in Example 1, starting with 4-trifluoromethoxy-2-methylaniline (0.65 g), potassium thiocyanate (1.3 g) and bromine (0.35 cc) in acetic acid (12 cc). After purification on a column of silica (200 g; particle size: 0.063-0.200 mm), eluting with a cyclohexane/ethyl acetate mixture (50:50 by volume), the white solid obtained (0.65 g) is ground in cyclohexane (20 cc), drained and dried at 60° C. under reduced pressure (1 mm Hg; 0.13 kPa), to give 4-methyl-6-trifluoromethoxy-2-benzothiazolamine (0.6 g), m.p. 162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05236940
Source datasetuspto-grants-1993_08
ORD IDord-cc58156e459b4f3b876305daae925f44
Source noteuspto-grants-1993_08