HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637870Generated: October 26, 2026
Thionyl Chloride → 2-Phenylbenzenesulfonyl isothiocyanate
https://huagongshe.com/reaction/637870
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 13422022 | HCID 13422022 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Phenylbenzenesulfonyl isothiocyanate | HCID 13422027 | — |
Reaction Steps
77 g of potassium N-(2-biphenylylsulfonyl)carbonimidodithioate prepared in accordance with Example 2 was suspended in 100 ml of toluene, and 37 ml of thionyl chloride was added to the suspension at 0° to 10° C. over the course of 1 hour. After the addition, the mixture was stirred at room temperature for 2 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. Distillation at reduced pressure gave 2-phenylbenzenesulfonyl isothiocyanate. On the other hand, 12.3 g of 2-amino-4,6-dimethylpyrimidine was suspended in 300 ml of dry toluene, and 27.5 g of 2-phenylbenzenesulfonyl isothiocyanate prepared as above was added. The mixture was heated under reduced pressure for 8 hours. After cooling, the resulting white precipitate was collected by filtration, and recrystallized from ethanol to give 31 g of the desired 1-(2-biphenylsulfonyl)3-(4,6-dimethylpyrimidin-2-yl)thiourea of the following formula, mp. 203°-204° C.: ##STR20##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04559079 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-f7288056c5d74c808da8f35e1016e01b |
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| Source note | uspto-grants-1985_12 |
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