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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | 5-tert-Butyl-2-methylaniline | HCID 13089979 | — |
| Reactant | CID 86753328 | HCID 86753328 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 5-tert-Butyl-2-methyl-4-thiocyanato-phenylamine | HCID 10751424 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834506 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-853d8691c3484b3c9c3c12f2e99bfcc6 |
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| Source note | uspto-grants-1998_11 |
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