Adamantane → 1-Bromoadamantane

HRID 1978106Notes

Reaction equation

HRID 1978106 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]2

Participants

3

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

  1. distillationsurplus bromine was distilled off under reduced pressure
  2. 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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