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

3-Methyl-8-methylidene-1,2,4,5,6,7,8,8a-octahydroazulen-6-ol → 6-Hydroxy-1,4-dimethyl-2,3,3a,4,5,6,7,8-octahydroazulene

HRID 597314
ノート
印刷プレビュー

反応式

HRID 597314 の反応式
[OH:1][CH:2]1[CH2:11][CH2:10][C:9]2[CH:5]([CH2:6][CH2:7][C:8]=2[CH3:12])[C:4](=[CH2:13])[CH2:3]1.[H][H]>C(O)C.[Pt]=O>[OH:1][CH:2]1[CH2:11][CH2:10][C:9]2[CH:5]([CH2:6][CH2:7][C:8]=2[CH3:12])[CH:4]([CH3:13])[CH2:3]1
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 214348863-Methyl-8-methylidene-1,2,4,5,6,7,8,8a-octahydroazulen-6-olHCID 178418361HCID 178418361、化合物

生成物 1

HCID 214349076-Hydroxy-1,4-dimethyl-2,3,3a,4,5,6,7,8-octahydroazulene収率 60.1%

試薬・触媒・溶媒 2

HCID 82844Platinum oxide (PtO)触媒HCID 702Ethanol溶媒

実験手順

500 mg of platinum oxide were pre-hydrogenated in 300 ml of ethanol. After addition of 2.14 g of 6-hydroxy-1-methyl-4-methylen-2,3,3a, 4,5,6,7,8-octahydroazulene, the mixture was hydrogenated until hydrogen was no longer taken up. The reaction mixture was filtered, the filtrate evaporated and the crude product distilled under reduced pressure in a bulb-tube. There were obtained 1.3 g of pure 6-hydroxy-1,4-dimethyl-2,3,3a, 4,5,6,7,8-octahydroazulene; b.p.0.001 ca 85°; IR(film):νmax 3380, 1460, 1440, 1095, 1078, 1035/30, 985/75, 940 cm-1. The substance has a woody, flowery, fresh green odour.

後処理

  1. filtrationThe reaction mixture was filtered
  2. customthe filtrate evaporated
  3. distillationthe crude product distilled under reduced pressure in a bulb-tube

出典と根拠

ORDレコード
ord-dece4b05fa834736bd181ddbd88e5518
出典データセット
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04013711

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