HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502608Generated: October 27, 2026
Sulfuryl chloride → 4-Chloro-2,3-dihydro-1,2-benzothiazol-3-one
https://huagongshe.com/reaction/502608
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | (NE)-N-[(2-chloro-6-methylsulfanylphenyl)methylidene]hydroxylamine | HCID 17910216 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-2,3-dihydro-1,2-benzothiazol-3-one | HCID 57436560 | — |
Reaction Steps
(E)-2-Chloro-6-(methylthio)benzaldehyde oxime (12.37 g) was dissolved in toluene (35 mL). Sulfuryl chloride (5.4 ml, 66.24 mmol) was added, dropwise to the solution at 0° C., followed by heating at 80° C. for 1 h. After the completion of the reaction, the reaction mixture was cooled to room temperature and a white precipitate formed. The solid was collected by vacuum filtration, washed with toluene and air dried to 4-chlorobenzo[d]isothiazol-3(2H)-one (6 g). (This method is general for other 2-(methythio) benzaldehyde oximes.) 1H NMR (300 MHz, DMSO-d6): 7.90 (t, 1H), 7.55 (t, 1H), 7.41 ppm (d, 1H). MW=186 confirmed by LC-MS, tr=2.38 min (Method B) MH+=187.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776847B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-dfacf1a4ce5644e48c25069af136a072 |
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| Source note | uspto-grants-2010_08 |
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