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

HCID 14467914、化合物 → HCID 58659580、化合物

HRID 854115
ノート
印刷プレビュー

反応式

HRID 854115 の反応式
N1C=CC=[CH:3][C:2]=1[CH2:7][S@@:8]([C:10]([CH3:13])([CH3:12])[CH3:11])=[O:9].N1C=CC=C[C:15]=1C[Li]>C1COCC1>[CH2:7]([S@:8]([C:10]([CH3:11])([CH3:12])[CH3:13])=[O:9])[CH:2]([CH3:3])[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

4

反応物 2

HCID 14467914HCID 14467914、化合物HCID 178506852HCID 178506852、化合物

生成物 1

HCID 58659580HCID 58659580、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Preparation of (S)-picolinyl t-butylsulfoxide from (S)-tert-Butyl (1R, 2S)-aminoindanol 4-toluene sulfonamide sulfinate: To a picolinyl lithium solution (2 mL, 0.6 M) in THF at −78° C. was added (S)-t-butyl-(1R, 2S)-aminoindanol tosylate sulfinate (130 mg, 0.30 mmol). The mixture was warmed to room temperature and stirred until the starting material was consumed as monitored by TLC. The reaction was quenched by aq. NaHCO3 (20 mL) and diluted with ethyl acetate (20 mL), and the organic phase was washed with water (20 mL) and brine (20 mL). The organic layer was concentrated in vacuo and the residue was purified by chromatography eluted with ethyl acetate to yield 32 mg of the desired product.

後処理

  1. customwas consumed
  2. customThe reaction was quenched by aq. NaHCO3 (20 mL)
  3. additiondiluted with ethyl acetate (20 mL)
  4. washthe organic phase was washed with water (20 mL) and brine (20 mL)
  5. concentrationThe organic layer was concentrated in vacuo
  6. customthe residue was purified by chromatography
  7. washeluted with ethyl acetate

出典と根拠

ORDレコード
ord-5ccc389c81d04c8caf6bfead3b78ebf8
出典データセット
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07256297B2

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