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

Sodium hydride → HCID 90087791、化合物

HRID 1486438
ノート
印刷プレビュー

反応式

HRID 1486438 の反応式
COP([CH2:7][C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])(OC)=O.[H-].[Na+].[F:17][C:18]([F:24])([F:23])[CH:19]([CH3:22])[CH:20]=O>C1COCC1>[F:17][C:18]([F:24])([F:23])[CH:19]([CH3:22])/[CH:20]=[CH:7]/[C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9]
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

5

反応物 3

HCID 24758Sodium hydrideHCID 27821883,3,3-trifluoro-2-methylpropanalHCID 4564495tert-Butyl Dimethylphosphonoacetate

生成物 1

HCID 90087791HCID 90087791、化合物収率 40.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒3 回

反応条件

温度
0 °C

実験手順

A solution of tert-butyl 2-(dimethoxyphosphoryl)acetate (9.78 g, 43.6 mmol) in THF (10 mL) was slowly transferred to a suspension of NaH (60% dispersion in mineral oil) (1.903 g, 47.6 mmol) in THF (30 mL) at 0° C. under a nitrogen atmosphere. After the addition was complete, the reaction mixture was stirred at 0° C. for 10 min, and then warmed to room temperature. After being stirred for 30 min, the reaction mixture was cooled to 0° C. again, and a solution of 3,3,3-trifluoro-2-methylpropanal (5 g, 39.7 mmol) in THF (10 mL) was added, and the ice bath was removed. After 12 h at 25° C., the mixture was partitioned between water (60 mL) and EtOAc (60 mL). The aqueous layer was extracted with EtOAc (60 mL), and the combined organic layers were successively washed with water (60 mL) and brine. The resulting solution was dried over MgSO4, concentration under reduced pressure, and purified by silica gel flash chromatography (330 g column, 0% to 15% EtOAc in hexane over 20 min) to obtain Intermediate S-5A (3.61 g, 16.10 mmol, 40.6% yield). 1H NMR (400 MHz, chloroform-d) δ 6.77 (dd, J=15.8, 7.7 Hz, 1H), 5.95 (dd, J=15.7, 0.6 Hz, 1H), 3.12-2.93 (m, 1H), 1.56-1.47 (m, 9H), 1.37-1.27 (m, 3H).

後処理

  1. additionAfter the addition
  2. temperaturewarmed to room temperature
  3. stirringAfter being stirred for 30 min
  4. temperaturethe reaction mixture was cooled to 0° C. again
  5. customthe ice bath was removed
  6. waitAfter 12 h at 25° C.
  7. customthe mixture was partitioned between water (60 mL) and EtOAc (60 mL)
  8. extractionThe aqueous layer was extracted with EtOAc (60 mL)
  9. washthe combined organic layers were successively washed with water (60 mL) and brine
  10. dry with materialThe resulting solution was dried over MgSO4, concentration under reduced pressure
  11. custompurified by silica gel flash chromatography (330 g column, 0% to 15% EtOAc in hexane over 20 min)
  12. customto obtain Intermediate S-5A (3.61 g, 16.10 mmol, 40.6% yield)

出典と根拠

ORDレコード
ord-8f37d829e76a42a58dce25741aabce62
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09427442B2

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