Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 53931004 | HCID 53931004 | — |
| Solvent | Bromochloromethane | HCID 6333 | — |
| Product | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 23450653 | HCID 23450653 | — |
Reaction Steps
Under a slight stream of nitrogen, 18.4 g of (2-chloro-allyl)-dithiocarbamic acid phenyl ester are placed in 100 ml of bromochloromethane and cooled to 0-1° C. Before and during the addition of bromine, the apparatus is flushed thoroughly with nitrogen. 13.8 g of bromine are added in the course of 120 minutes in such a manner that the temperature can be maintained at 0-10° C. When the addition is complete, stirring is carried out for about 20 minutes. The reaction mixture is concentrated in vacuo at 20-25° C. 50 ml of hexane are added to the residue, and the product is filtered off with suction at 20-25° C., washed with 30 ml of hexane and dried in vacuo at room temperature. The title product is obtained in the form of the hydrobromide (compound 2.2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06369233B1 |
|---|
| Source dataset | uspto-grants-2002_04 |
|---|
| ORD ID | ord-1f8719833e0f4b099368f0a22f9ac576 |
|---|
| Source note | uspto-grants-2002_04 |
|---|