Adamantane → 1-Bromoadamantane
Reaction equation
[CH:1]12[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.[Br:11]Br>>[Br:11][C:1]12[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2Participants
3
Reactant 2
Product 1
Procedure
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.
Workup
- distillationsurplus bromine was distilled off under reduced pressure
- additionafter the addition of 200 ml of carbon tetrachloride (IV)
Sources & evidence
- ORD record
- ord-1a18148b9a2c47c9b55b3e03dfe6fb32
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06235851B1
Reaction notes
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