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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356516Generated: October 27, 2026

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

https://huagongshe.com/reaction/356516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium BromideHCID 253881—
Reactant5-tert-Butyl-2-methylanilineHCID 13089979—
ReactantCID 86753328HCID 86753328—
SolventMethanolHCID 887—
SolventSodium BicarbonateHCID 516892—
Product5-tert-Butyl-2-methyl-4-thiocyanato-phenylamineHCID 10751424—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1.0 g (6.1 mmol) of 5-tert-butyl-2-methyl-phenylamine prepared in Example CCCC, sodium thiocyanide (1.62 g, 20.0 mmol) and MeOH (4.0 mL) was cooled to 0° C. and treated via addition funnel with a solution of bromine (0.35 mL, 6.7 mmol), sodium bromide (0.63 g, 6.13 mmol), and MeOH (5.0 mL). The mixture was stirred for 30 minutes and then carefully diluted with saturated sodium bicarbonate. The mixture was extracted with CH2Cl2 and the organic layers combined, dried (Na2SO4), and the solvent evaporated. The residue was then submitted to column chromatography (4:1 CH2Cl2 :hexanes to 19:1 CH2 C12 :hexanes+1% MeOH) to provide the title compound. 1H NMR (CDCl3) δ 1.42 (s, 9 H), 2.09 (s, 3 H), 3.80 (bs, 2 H), 6.69 (s, 1 H), 7.35 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834506
Source datasetuspto-grants-1998_11
ORD IDord-853d8691c3484b3c9c3c12f2e99bfcc6
Source noteuspto-grants-1998_11