HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → ((2-Bromoethyl)thio)cyclohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Cyclohexanethiol | HCID 15290 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ((2-Bromoethyl)thio)cyclohexane | HCID 22455667 | — |
Reaction Steps
19.4 ml (225.0 mmol) of 1,2-dibromoethane and 4.1 g (30.0 mmol) of K2CO3 were added to a solution of 3.7 ml (30.0 mmol) of cyclohexanethiol in DMF (46 ml). After 2 hours of stirring at RT, the mixture was diluted with diethyl ether (200 ml) and washed with saturated aqueous NaCl solution. The organic phase was dried over MgSO4, filtered and concentrated in vacuo. The resulting 6.1 g of crude product (2-bromoethyl)(cyclohexyl)sulfane were used for the further reaction without being purified further.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084470B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-dd396bdeb76849959566f21f60b0b23d |
| Source note | uspto-grants-2011_12 |