HuagongsheHuagongshe Chemistry Print Report · For research reference only
Adamantane → 1-Bromoadamantane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Adamantane | HCID 9238 | — |
| Reactant | Bromine | HCID 24408 | — |
| Product | 1-Bromoadamantane | HCID 79106 | — |
Reaction Steps
The reaction was conducted in accordance with the method of The Japanese Patent Publication No. 61980/1995 (JP-B-7-61980) to obtain an adamantane monoaclylate, namely, 15 mole of anhydrousbromine and 1.6 mole of adamantane were reacted at the reflux temperature of bromine for 7 hours, surplus bromine was distilled off under reduced pressure, and after the addition of 200 ml of carbon tetrachloride (IV), the residual bromine was resolved with sodium sulfite. A white powderly 1-bromoadamantane was provided by removing organic layer, and recrystallizing the obtained crude products from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235851B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-1a18148b9a2c47c9b55b3e03dfe6fb32 |
| Source note | uspto-grants-2001_05 |