HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloromethanethiol → 5-Chloro-3-p-tolyl-[1,2,4]thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloromethanethiol | HCID 6390 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methylbenzene-1-carboximidamide hydrochloride | HCID 122753 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Chloro-3-p-tolyl-[1,2,4]thiadiazole | HCID 22611066 | 44% |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
To a mixture of p-methylbenzamidine hydrochloride (5.1 g, 30.0 mmol) in CHCl3 (100 ml) is added triethyl amine (15.12 g, 20.9 ml, 150.0 mmol) and cooled to 5° C. in an ice-water bath. To the mixture is slowly added perchloromethyl mercaptan (95%, 6.16 g, 31.5 mmol) in CHCl3(10 ml) over 1 hour. The yellow solution is allowed to warm up to room temperature. After 2 hours the mixture is washed with water (100 ml×2) and brine (100 ml). The organic layer is dried over MgSO4 and the solvent is removed under reduced pressure to yield a brown oil. The oil is purified on a bed of silica gel, eluting with 1:1 CHCl3:hexanes to yield 3-(p-tolyl)-5-chloro-1,2,4-thiadiazole as a yellow solid (2.78 g, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380187B2 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-be99e0bc80fc484f861a3e904e98a3c2 |
| Source note | uspto-grants-2002_04 |