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

m-Chloroperbenzoic acid → HCID 15332454、化合物

HRID 487517
ノート
印刷プレビュー

反応式

HRID 487517 の反応式
ClC1C=C(C=CC=1)C(OO)=[O:6].[CH3:12][C:13]([CH2:15][CH:16]([CH3:23])[CH2:17][CH:18]([CH3:22])[CH2:19][CH2:20][CH3:21])=[CH2:14]>C(Cl)Cl>[CH3:14][C:13]1([CH2:15][CH:16]([CH3:23])[CH2:17][CH:18]([CH3:22])[CH2:19][CH2:20][CH3:21])[O:6][CH2:12]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 5361182,4,6-Trimethyl-1-nonene

生成物 1

HCID 15332454HCID 15332454、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
10 °C

実験手順

m-Chloroperoxybenzoic acid (7.31 g, 60% purity, 25.42 mmol) was added to a stirred solution of 2,4,6-trimethyl-1-nonene (5) (3.56 g, 21.19 mmol) in 70 ml of dry methylene chloride in a 250 ml flask in an ice bath. The chilled reaction mixture was stirred for one hour, and then stirred vigorously overnight at room temperature. The reaction mixture was cooled to 10° C. before filtering out a white slurry, which was washed with cooled methylene chloride. The combined filtrates were washed three times with cooled aqueous carbonate, water, and brine and dried over sodium sulfate. Evaporation of the solvent yielded a crude oil which was distilled at 65°-70° C. and 1.5 mm Hg to yield pure 2,4,6-trimethyl-1,2-epoxynonane (6).

後処理

  1. customThe chilled reaction mixture
  2. stirringstirred vigorously overnight at room temperature
  3. filtrationbefore filtering out a white slurry, which
  4. washwas washed with cooled methylene chloride
  5. washThe combined filtrates were washed three times with cooled aqueous carbonate, water, and brine
  6. dry with materialdried over sodium sulfate
  7. customEvaporation of the solvent
  8. customyielded a crude oil which
  9. distillationwas distilled at 65°-70° C.

出典と根拠

ORDレコード
ord-9371c626af0e4c8299d2837964360e61
出典データセット
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05296220

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート