HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 570562Erstellt: 23. Oktober 2026
Trichloromethanethiol → 5-Chloro-3-p-tolyl-[1,2,4]thiadiazole
https://huagongshe.com/de/reaction/570562
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trichloromethanethiol | HCID 6390 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Methylbenzene-1-carboximidamide hydrochloride | HCID 122753 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-Chloro-3-p-tolyl-[1,2,4]thiadiazole | HCID 22611066 | 85,2% |
Reaktionsschritte
A mixture of 4-methylbenzimidamide hydrochloride (1.55 g, 9.08 mmol) and Et3N (4.6 g, 6.33 ml, 45.4 mmol) in DCM (30 mL) was cooled with a NaCl/ice-bath to −10° C. Perchloromethyl mercaptan (1.86 g, 1.09 ml, 9.99 mmol) in DCM (10 mL) was added during 40 min. The resulting yellow suspension was stirred for 20 min at 0° C. and 2 h at RT. Water (40 mL) and aq. 2N NaOH (10 mL) was added. The organic layer was separated and extracted with brine (50 mL). The aqueous layers were extracted with DCM (2×40 mL). The combined organic layers were dried over Na2SO4, filtered off and concentrated in vacuo. The residue was purified by silica chromatography (Flash 50 g Si-cartridge using AcOEt: Heptane 1:19 to 1:9.) to yield 5-chloro-3-p-tolyl-1,2,4-thiadiazole (1.63 g, 7.74 mmol, 85% yield) as light yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09023852B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-af8ea00295e94d8694bd585418025f97 |
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| Quellennotiz | uspto-grants-2015_05 |
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