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

Isopropanol → Octane

HRID 2049514
ノート
印刷プレビュー

反応式

HRID 2049514 の反応式
[Ni:1].CO.[C:4]([CH:8]1[C:15](C(C)(C)C)(O)[CH:14]=[CH:13][C:10]([CH2:11][OH:12])=[CH:9]1)(C)(C)[CH3:5].CC(O)C>C1C=CC=CC=1>[Ni:1].[CH3:11][OH:12].[CH3:5][CH2:4][CH2:8][CH2:9][CH2:10][CH2:13][CH2:14][CH3:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 3776IsopropanolHCID 22477019Nickel monomethoxideHCID 705893803,4-Di-t-butyl-4-hydroxybenzyl alcohol

生成物 2

HCID 356OctaneHCID 22477019Nickel monomethoxide

試薬・触媒・溶媒 1

HCID 241Benzene溶媒2 回

実験手順

[2,2'-thiobis-(4-t-octylphenolato)]-2-propanol nickel II (83.9 g) prepared as described in Example 4 was dissolved in benzene (250 ml) and 3,4-di-t-butyl-4-hydroxybenzyl alcohol (35.5 g) was added. The temperature of the mixture was raised to reflux and the resulting solution was refluxed for 2.25 hr. Displaced 2-propanol and benzene (150 ml) were then distilled from the reaction mixture. Remaining solvent was removed by rotary evaporation. From the residue the complex [2,2'-thiobis-(4-t-octylphenolato)]-3,4-di-t-butyl-4-hydroxybenzyl alcohol nickel II was obtained by recrystallization from n-octane as a green solid m.p. 253°-255° C.

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

後処理

  1. temperatureThe temperature of the mixture was raised
  2. temperatureto reflux
  3. temperaturethe resulting solution was refluxed for 2.25 hr
  4. distillationwere then distilled from the reaction mixture
  5. customRemaining solvent was removed by rotary evaporation

出典と根拠

ORDレコード
ord-e9ec0fe38c8b486fa01b6538020fda03
出典データセット
uspto-grants-1980_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04198303

反応ノート

読み込み中…