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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 5-tert-Butyl-o-cresol | HCID 79845 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | CID 86753328 | HCID 86753328 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-tert-Butyl-2-methyl-4-thiocyanato-phenol | HCID 10560955 | — |
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
| 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-aefea9b903b04ba99103150098733d61 |
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| Source note | uspto-grants-1998_11 |
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