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

Acetic Acid → 2-(3-Fluoro-4-(2-nitro-ethyl)-phenoxymethyl)-pyridine

HRID 640359
ノート
印刷プレビュー

反応式

HRID 640359 の反応式
CS(C)=O.[F:5][C:6]1[CH:7]=[C:8]([CH:17]=[CH:18][C:19]=1/[CH:20]=[CH:21]/[N+:22]([O-:24])=[O:23])[O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][N:12]=1.C(O)(=O)C.[BH4-].[Na+]>O>[F:5][C:6]1[CH:7]=[C:8]([CH:17]=[CH:18][C:19]=1[CH2:20][CH2:21][N+:22]([O-:24])=[O:23])[O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][N:12]=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 176Acetic AcidHCID 679Dimethyl SulfoxideHCID 4311764Sodium borohydrideHCID 592552272-(3-Fluoro-4-((E)-2-nitro-vinyl)-phenoxymethyl)pyridine

生成物 1

HCID 592554052-(3-Fluoro-4-(2-nitro-ethyl)-phenoxymethyl)-pyridine収率 50.8%

試薬・触媒・溶媒 1

HCID 962
Water
溶媒

実験手順

To a dimethyl sulfoxide (20.0 mL) solution of 2-(3-fluoro-4-((E)-2-nitro-vinyl)-phenoxymethyl)pyridine (1.20 g) described in Manufacturing Example 95-1-2 and acetic acid (1.00 mL) was added sodium borohydride (249 mg, 6.57 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 30 minutes at room temperature. Water was then added dropwise at room temperature while cooling appropriately. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, followed by crystallization with an ethyl acetate-heptane system and filtration to obtain the title compound (614 mg, 50.7%).

後処理

  1. temperaturewhile cooling appropriately under nitrogen atmosphere
  2. temperaturewhile cooling appropriately
  3. extractionThe reaction mixture was extracted with ethyl acetate
  4. washthe organic layer was washed with water and saturated aqueous sodium chloride
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated under a reduced pressure
  8. customfollowed by crystallization with an ethyl acetate-heptane system and filtration

出典と根拠

ORDレコード
ord-a6497efaac9048968bfb072ba48dcaa3
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07691882B2

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