ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Water → 8-Methyl-3,8-diazabicyclo(3.2.1)octane dihydrochloride

HRID 268218
ノート
印刷プレビュー

反応式

HRID 268218 の反応式
O.[ClH:2].Cl.C([N:11]1[CH2:17][CH:16]2[N:18]([CH3:19])[CH:13]([CH2:14][CH2:15]2)[CH2:12]1)C1C=CC=CC=1.O>C(O)C.[Pd]>[ClH:2].[ClH:2].[CH3:19][N:18]1[CH:13]2[CH2:14][CH2:15][CH:16]1[CH2:17][NH:11][CH2:12]2
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 962WaterHCID 215454913-Benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane dihydrochloride monohydrate

生成物 1

HCID 221201898-Methyl-3,8-diazabicyclo(3.2.1)octane dihydrochloride収率 152.9%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

A mixture of 3-benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane dihydrochloride monohydrate (18.1 g, 0.059 mole) in absolute ethanol (200 ml) and 10% palladium on charcoal (3.0 g) was hydrogenated for 2 hours at atmospheric pressure. Sufficient water was added to dissolve the insoluble hydrochloride salt that had formed, and the reaction was filtered. The filtrate was evaporated in vacuo, the residue was triturated in hot absolute ethanol, and the mixture was filtered to yield 8.98 g of 8-methyl-3,8-diazabicyclo[3.2.1]octane dihydrochloride, melting point 315°C (dec.). The mother liquor was treated with ethanolic dry hydrogen chloride to afford an additional 2.28 g. Yield: 12.26 g (96%).

後処理

  1. customhad formed
  2. filtrationthe reaction was filtered
  3. customThe filtrate was evaporated in vacuo
  4. customthe residue was triturated in hot absolute ethanol
  5. filtrationthe mixture was filtered

出典と根拠

ORDレコード
ord-e60ddb19b937414ebb6aed244c29f12b
出典データセット
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03947445

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート