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

Tetrahydrofuran → 4-(1,1-Dimethyl-4,4,4-trifluoro-2-butynyl)anisole

HRID 2269265
ノート
印刷プレビュー

反応式

HRID 2269265 の反応式
[Li][CH2:2]CCC.[F:6][C:7]([F:13])([F:12])S([O-])(=O)=O.FC(F)(F)[S+]1[C:20]2C=C[CH:23]=[CH:24][C:19]=2[C:18]2[CH:25]=[CH:26][CH:27]=[CH:28][C:17]1=2.C1C[O:34][CH2:33]C1>>[CH3:2][C:19]([C:18]1[CH:17]=[CH:28][C:27]([O:34][CH3:33])=[CH:26][CH:25]=1)([CH3:20])[C:24]#[C:23][C:7]([F:13])([F:12])[F:6]
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 3

HCID 8028TetrahydrofuranHCID 27775075-(Trifluoromethyl)dibenzothiophenium trifluoromethanesulfonateHCID 178418339Butyllithium

生成物 1

HCID 186775904-(1,1-Dimethyl-4,4,4-trifluoro-2-butynyl)anisole収率 13%

反応条件

温度
0 °C

実験手順

To a stirred solution of Compound 56 (0.22 g, 1.26 mmol) in THF (8 ml) was added n-BuLi (1.69 M in hexane, 0.82 ml, 1.39 mmol) at −78° C. under N2, then warmed up to 0° C., and stirred for 1 h. S-(Trifluoromethyl)dibenzothiophenium trifluoromethane-sulfonate (1.01 g, 2.52 mmol) was added, and stirred for 3 h at 0° C. The mixture was quenched by the addition of NaHCO3 aq., and extracted with CH2Cl2. The combined organic layers were dried over MgSO4, filtered, and concentrated. This was purified by SiO2 chromatography to give Compound 57 (38 mg, 13%) as a colorless oil.

後処理

  1. stirringstirred for 3 h at 0° C
  2. customThe mixture was quenched by the addition of NaHCO3 aq.
  3. extractionextracted with CH2Cl2
  4. dry with materialThe combined organic layers were dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThis was purified by SiO2 chromatography

出典と根拠

ORDレコード
ord-65b09b873966426fb341b59ac38de3fc
出典データセット
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06329396B1

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