HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242003Generated: October 28, 2026
1-Bromo-2-Chloroethane → 5-(2-Chloroethoxy)-2-methylthio-benzothiazole
https://huagongshe.com/reaction/1242003
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Benzothiazolol,2-(methylthio)-(9CI) | HCID 21937628 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(2-Chloroethoxy)-2-methylthio-benzothiazole | HCID 21937487 | 46% |
Reaction Steps
To a solution of 5-hydroxy-2-methylthio-benzothiazole (2.1 g, 11 mmol) in anhydrous DMF (25 mL) was added bromo-2-chloroethane (4.4 mL, 53 mmol) and powdered K2CO3 (7.3 g, 53 mmol). The reaction slurry was heated at 70° C. for 13 h. The slurry was filtered under vacuum and the filtrate was concentrated under reduced pressure. The crude material was chromatographed (SiO2, 0–20% EtOAc/Hex) to afford the title compound (1.2 g, 46%). 1H-NMR (CDCl3): δ 7.62 (1H, d), 7.39 (1H, d), 6.97 (1H, dd), 4.29 (2H, t), 3.85 (2H, t), 2.79 (3H, s); MS(ESI): 259(MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115640B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-f87b3f7d025b42ba981202e81a52169e |
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| Source note | uspto-grants-2006_10 |
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