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1-Methylbicyclo[2.2.1]heptan-2-ol → HCID 57313420、化合物

HRID 2211325
ノート
印刷プレビュー

反応式

HRID 2211325 の反応式
[CH3:1][C:2]12[CH2:8][CH:5]([CH2:6][CH2:7]1)[CH2:4][CH:3]2[OH:9].[H-].[Al+3].[Li+].[H-].[H-].[H-]>>[CH3:1][C@@:2]12[CH2:8][CH:5]([CH2:6][CH2:7]1)[CH2:4][CH:3]2[OH:9]
参加物実験手順出典と根拠反応ノート

参加物

3

反応物 2

HCID 5572391-Methylbicyclo[2.2.1]heptan-2-ol2 回HCID 21226445Aluminium lithium hydride

生成物 1

HCID 57313420HCID 57313420、化合物

実験手順

Norbornanone (I) is reacted with methylmagnesium iodide to give 2-methyl-2-norbornanol (II). The compound (II) is reacted with acetic acid and a 75% solution of sulfuric acid to give 2-acetoxy-1-methylnorbornane (III) which is then converted into 1-methyl- 2-norbornanol (IV) with lithium-aluminum hydride. Then the compound (IV) is enzymatically resolved according to the method reported by Christian Triantaphylides et al., Tetrahedron Letters, 26(15), 1857 (1985) to give (1S)-1-methyl-2-norbornanol (V). This optically active alcohol (V) is then oxidized with pyridine dichromate complex to give (1S)-1-methyl-2-norbornanone (VI). The compound (VI) is reacted with methyltriphenylphosphonium bromide in the presence of n-butyllithium to give (1S)-2-methylenenorbornane (VII) which is then treated with peracetic acid to give an epoxy compound. This epoxy compound is treated with a boron trifluoride etherate complex to give (1S,2S)-1-methyl-2-norbornyl aldehyde (VIII) which is then reduced with lithium aluminum hydride to give (1S,2S)-1-methyl-2-hydroxymethylnorbornane (IX).

出典と根拠

ORDレコード
ord-624e9ee8aa304763ad41fbfbd0d747cd
出典データセット
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05463118

反応ノート

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