反応式
[N-:1]=[N+:2]=[N-:3].[Na+].Br.Br[CH2:7][CH2:8][CH2:9][CH:10]1[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]1.O>CO>[N:1]([CH2:7][CH2:8][CH2:9][CH:10]1[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]1)=[N+:2]=[N-:3]参加物
5
実験手順
Sodium azide (1 g) was added to a mixture of 4-(3'-bromopropyl)-piperidine hydrobromide (2 g), water (7 ml) and methanol (7 ml). The pH of the mixture was adjusted to 6.3, and the resulting solution was refluxed for 2 hours. After cooling, methanol was evaporated, 30 percent aqueous sodium hydroxide was added and the mixture was extracted several times with ether. The ether extracts were dried and evaporated to leave the desired compound as an oil. The IR-spectrum (CHCl3) showed strong bands at 2925, 2100 and 1450 cm-1.
後処理
- temperaturethe resulting solution was refluxed for 2 hours
- temperatureAfter cooling
- custommethanol was evaporated
- addition30 percent aqueous sodium hydroxide was added
- extractionthe mixture was extracted several times with ether
- dry with materialThe ether extracts were dried
- customevaporated
出典と根拠
- ORDレコード
- ord-b781a9270d234d71a42cb93863da6b3f
- 出典データセット
- uspto-grants-1982_08
- 特許番号
- US04345071
関連ノート
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