反応式
[C:1]12([CH2:11]O)[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.C12(CBr)CC3CC(CC(C3)C1)C2.Br.[ClH:26]>[Br-].[Zn+2].[Br-].[Cl-].[Zn+2].[Cl-]>[C:1]12([CH2:11][Cl:26])[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2参加物
7
実験手順
Chlorination reaction of 1-adamantyl methylalcohol which was obtained by the same method described in (1) was carried out under the same conditions for the bromination reaction shown in (2) except that zinc bromide and hydrobromic acid were replaced by zinc chloride and hydrochloric acid respectively. The product was purified by recrystallized from methanol. Melting point of 1-adamantyl methyl chloride thus obtained was 32°-34° C and the yield was 91%.
後処理
- customwas obtained by the same method
- customwas carried out under the same conditions for the bromination reaction
- customThe product was purified
- customby recrystallized from methanol
出典と根拠
- ORDレコード
- ord-fbbd2f48596345ff98bd1e3f739e32b8
- 出典データセット
- uspto-grants-1977_01
- 特許番号
- US04001223
関連ノート
読み込み中…