Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Benzyl (2-chloroprop-2-en-1-yl)carbamodithioate | HCID 54395229 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 23450655 | HCID 23450655 | — |
Reaction Steps
Under a slight stream of nitrogen, 19.9 g of (2-chloro-allyl)-dithiocarbamic acid benzyl ester are placed in 100 ml of ethyl acetate and cooled to 0-1° C. During the addition of bromine, the apparatus is flushed thoroughly with nitrogen. 14.0 g of bromine are added in the course of 40 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 20-250C. 50 ml of hexane are added, the mixture is filtered at 20-25° C., and the filtration residue is washed with 40 ml of hexane and dried in vacuo at room temperature. The title product is obtained in the form of the hydrobromide (compound 2.1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06369233B1 |
|---|
| Source dataset | uspto-grants-2002_04 |
|---|
| ORD ID | ord-1efd337d0ebc4865b1881b0d13f9f6f3 |
|---|
| Source note | uspto-grants-2002_04 |
|---|