HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → S-methyl N-[N'-methyl-N'-(diisopropylaminosulfenyl)carbamoyloxy]thioacetimidate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-methyl-N-(diisopropylaminosulfenyl)carbamoyl fluoride | HCID 20551373 | — |
| Reactant | HCID 178504139 | HCID 178504139 | — |
| Catalyst | Dicyclohexano-18-crown-6 | HCID 85955 | — |
| Solvent | Water | HCID 962 | — |
| Product | S-methyl N-[N'-methyl-N'-(diisopropylaminosulfenyl)carbamoyloxy]thioacetimidate | HCID 54073397 | 67.3% |
Reaction Steps
Powdered potassium hydroxide (2.5 g), 4.7 g. 10.045 mole) of S-methyl-N-hydroxythioacetimidate, 0.11 g dicyclohexyl-18-crown-6, and benzene (200 mol) were combined and stirred 0.5 hr. at room temperature. Then 9.4 g (0.045 mole) of N-methyl-N-(diisopropylaminosulfenyl)carbamoyl fluoride were added. The mixure was stirred at room temperature for 1 hr., and then was water washed four times, dried (MgSO4), and the benzene solvent was removed under vacuum. The residue was recrystallized from diisopropyl ether to give 9 g (67.3 percent yield) of S-methyl N-[N'-methyl-N'-(diisopropylaminosulfenyl)carbamoyloxy]thioacetimidate, m.p. 79°-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04315928 |
| Source dataset | uspto-grants-1982_02 |
| ORD ID | ord-e978ca652bec4673983b17d8c5da3c44 |
| Source note | uspto-grants-1982_02 |