HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexane → HCID 15529886, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | t-Butyl bromide | HCID 10485 | — |
| Reactant | Bromhydrol | HCID 166749 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15529886 | HCID 15529886 | — |
Reaction Steps
Into a 200 ml egg plant-shaped flask, 8.8 g (0.046 moles) of 1-(n-butyl)adamantane obtained above was weighed and placed. Under the stream of nitrogen gas, 100 ml of cyclohexane was added, and a solution was prepared. While the solution was kept at 0° C. in an ice bath, 8.8 g (0.063 moles) of t-butyl bromide and 0.4 g (0.0014 moles) of aluminum bromide were added, and the reaction was allowed to proceed for 2 hours. To the reaction fluid, 100 ml of ion-exchanged water was added, and the extraction with cyclohexane was conducted using a separation funnel. The solvent was removed using an evaporator, and 10.4 g of 1-bromo-3-(n-butyl)adamantane of the object compound was obtained as a colorless transparent liquid substance (the yield: 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08337982B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-387b0780b0fb49569d37046cb9764b76 |
| Source note | uspto-grants-2012_12 |