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

Hydrogen Peroxide → (S)-2-(1,4-Dibenzylpiperazin-2-yl)ethanol

HRID 131395
ノート
印刷プレビュー

反応式

HRID 131395 の反応式
[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][C@@H:9]1[CH:21]=[CH2:22])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.B1C2CCCC1CCC2.[OH:32]O.[OH-].[Na+]>O1CCCC1>[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][C@@H:9]1[CH2:21][CH2:22][OH:32])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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 4

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 789669-Borabicyclo(3.3.1)nonaneHCID 17759473(S)-1,4-dibenzyl-2-vinylpiperazine

生成物 1

HCID 59732113(S)-2-(1,4-Dibenzylpiperazin-2-yl)ethanol収率 96%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran
溶媒
2 回

実験手順

Dissolve (S)-1,4-dibenzyl-2-vinylpiperazine (16.2 g, 55.5 mmol) in tetrahydrofuran (370 mL), add 9-BBN (0.56 L of a 0.5 M solution in tetrahydrofuran) via addition funnel, stir at room temperature overnight. Cool to 0° C. and treat with 30% aqueous hydrogen peroxide (195 mL), followed by 3N aqueous sodium hydroxide (195 mL). Allow to reach room temperature and stir for 24 h. Pour into separatory funnel, separate organic layer and remove solvent in vacuo. Take up residue in dichloromethane, add water and recombine with aqueous layer from before. Pour into separatory funnel, separate organic layer and extract aqueous layer with several portions of dichloromethane. Combine all organic layers, remove solvent in vacuo. Take up residue in 1 L of methanol, add 185 g of SCX resin. Filter slurry through Büchner funnel, washing well with methanol. To elute product, wash cake thoroughly with 50% 7N ammonia-methanol in dichloromethane. Concentrate filtrate in vacuo to obtain the title compound (16.6 g, 96%) as a thick brownish oil: mass spectrum (APCI): m/z=311.2 (M+1).

後処理

  1. additionvia addition funnel
  2. temperatureCool to 0° C.
  3. customto reach room temperature
  4. stirringstir for 24 h
  5. additionPour into separatory funnel
  6. customseparate organic layer
  7. customremove solvent in vacuo
  8. additionadd water and recombine with aqueous layer from before
  9. additionPour into separatory funnel
  10. customseparate organic layer
  11. extractionextract aqueous layer with several portions of dichloromethane
  12. customCombine all organic layers, remove solvent in vacuo
  13. additionadd 185 g of SCX resin
  14. filtrationFilter slurry through Büchner funnel
  15. washwashing well with methanol
  16. washTo elute product
  17. washwash cake thoroughly with 50% 7N ammonia-methanol in dichloromethane

出典と根拠

ORDレコード
ord-f360a5f709474baeb5b9199f00ab6fa6
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07384934B2

反応ノート

読み込み中…

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