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

Hydrochloric Acid → Benzene, 1-(1,1-dimethylethoxy)-4-fluoro-2-nitro-

HRID 2167448
ノート
印刷プレビュー

反応式

HRID 2167448 の反応式
O1CCCC1.[CH3:6][C:7]([CH3:10])([O-:9])[CH3:8].[K+].F[C:13]1[CH:18]=[CH:17][C:16]([F:19])=[CH:15][C:14]=1[N+:20]([O-:22])=[O:21].Cl>O>[C:7]([O:9][C:13]1[CH:18]=[CH:17][C:16]([F:19])=[CH:15][C:14]=1[N+:20]([O-:22])=[O:21])([CH3:10])([CH3:8])[CH3:6]
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 313Hydrochloric AcidHCID 8028TetrahydrofuranHCID 677672,5-DifluoronitrobenzeneHCID 23665647Potassium tert-butoxide

生成物 1

HCID 11680099Benzene, 1-(1,1-dimethylethoxy)-4-fluoro-2-nitro-収率 80%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

A tetrahydrofuran (THF) solution (20 ml) of potassium tert-butoxide (3.55 g, 31.6 mmol) was cooled in an methanol-ice bath, and 4.2 g of 2,5-difluoronitrobenzene (26.4 mmol) was further added. The mixture was heated to room temperature, stirred for 96 hours, and further stirred at 60° C. for 1 hour. Water (2 ml) and 2N-hydrochloric acid (2 ml) were added to the reaction mixture while cooling with an ice water bath, and subsequently water was added. The resulting mixture was extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the residue was then purified using silica gel column chromatography (n-hexane:ethyl acetate=19:1). The purified product was concentrated under reduced pressure to thereby obtain 4.5 g of oily orange 1-tert-butoxy-4-fluoro-2-nitrobenzene (yield: 80%).

後処理

  1. stirringfurther stirred at 60° C. for 1 hour
  2. temperaturewhile cooling with an ice water bath
  3. extractionThe resulting mixture was extracted with ethyl acetate
  4. concentrationThe organic layer was concentrated under reduced pressure
  5. customthe residue was then purified
  6. concentrationThe purified product was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-9cfdd2a16e4d463b95b4f6c6c8521f5c
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09045464B2

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