m-Chloroperbenzoic acid → 1,2-Epoxy-1-(4-nonylphenyl)-hexane

HRID 2231854

反応式

HRID 2231854 の反応式
ClC1C=CC=C(C(OO)=[O:9])C=1.[CH2:12]([C:21]1[CH:26]=[CH:25][C:24]([CH:27]=[CH:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH:23][CH:22]=1)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]>ClCCl>[O:9]1[CH:28]([CH2:29][CH2:30][CH2:31][CH3:32])[CH:27]1[C:24]1[CH:23]=[CH:22][C:21]([CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])=[CH:26][CH:25]=1

参加物

4

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 536769591-(4-Nonylphenyl)-hex-1-ene

生成物 1

HCID 212731161,2-Epoxy-1-(4-nonylphenyl)-hexane

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

6.76 g of m-chloroperbenzoic acid (90% content) in 100 ml of dichloromethane are added to a solution of 6.32 g of 1-(4-nonylphenyl)-hex-1-ene (mixture of cis- and trans-isomers) from the preceding stage in 150 ml of dichloromethane while cooling to 0°-5°, and the whole is stirred for 20 hours at 20°. The reaction mixture is washed in succession with 10% strength (w/v) sodium sulphite solution, 5% strength (w/v) sodium carbonate solution and 3 portions of water, dried over sodium sulphate and concentrated by evaporation. Chromatography of the residue on silica gel with hexane/ethyl acetate (19:1) yields in succession the trans- [1(RS),2(RS)-] and the cis-[1(RS),2(SR)-]-isomer in the form of colourless oils.

後処理

  1. temperaturewhile cooling to 0°-5°
  2. washThe reaction mixture is washed in succession with 10% strength (w/v) sodium sulphite solution, 5% strength (w/v) sodium carbonate solution and 3 portions of water
  3. dry with materialdried over sodium sulphate
  4. concentrationconcentrated by evaporation
  5. customChromatography of the residue on silica gel with hexane/ethyl acetate (19:1) yields in succession the trans- [1(RS),2(RS)-]

出典と根拠

ORDレコード
ord-e1b5a0c595034ae3945e7765def8bcd4
出典データセット
uspto-grants-1988_11
特許番号
US04785004

関連ノート

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