HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729172Generated: November 1, 2026
2-(methylamino)benzenethiol → HCID 15027933, compound
https://huagongshe.com/reaction/1729172
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(methylamino)benzenethiol | HCID 452161 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 15027913 | HCID 15027913 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 15027933 | HCID 15027933 | — |
Reaction Steps
4.5 g (=0.032 m) of 2-(methylamino)-thiophenol, 6 g of triethylbenzylammonium chloride, and 11.20 g of sodium hydrogen carbonate were added to 120 ml of chloroform. The resulting suspension was cooled to 5° C., and then a solution of 10.88 g of 2,6-dibromohexanoyl bromide in 20 ml of chloroform was added dropwise so slowly that the temperature did not exceed 5° C. 20 minutes were required for the addition. The reaction mixture was then allowed to warm to room temperature and was subsequently heated under reflux for 4 hours. The reaction mixture was worked up by cooling and filtering it. The chloroform phase was washed, dried over sodium sulfate, and the solvent was distilled off. The 2-(4-bromobutyl)-4-methyl-2H-1,4-benzothiazine-3(4H)-one which formed was isolated from the remaining residue by fractional column chromatography. 2.78 g of white crystals having a melting point of 116° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05332733 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-50aeeaf9ee8b401b9400658386da7065 |
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| Source note | uspto-grants-1994_07 |
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