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

Nitric Acid → 3-Nitro-5-pentafluorosulfanylbenzoic Acid

HRID 217757
ノート
印刷プレビュー

反応式

HRID 217757 の反応式
[F:1][S:2]([F:15])([F:14])([F:13])([F:12])[C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][CH:11]=1)[C:6]([OH:8])=[O:7].S(=O)(=O)(O)O.[N+:21]([O-])([OH:23])=[O:22]>>[F:1][S:2]([F:12])([F:13])([F:14])([F:15])[C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([N+:21]([O-:23])=[O:22])[CH:11]=1)[C:6]([OH:8])=[O:7]
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 3

HCID 944Nitric AcidHCID 1118Sulfuric Acid2 回HCID 27792093-(Pentafluorosulfanyl)benzoic acid

生成物 1

HCID 596421523-Nitro-5-pentafluorosulfanylbenzoic Acid

実験手順

3-Pentafluorosulfanylbenzoic acid (15 g) was dissolved in fuming nitric acid (120 ml) and stirred at RT with exclusion of moisture. Then concentrated sulfuric acid (7.5 ml) was added and the mixture was stirred at 75° C. After stirring at 75° C. for 8 h, the mixture was left to stand overnight, then further sulfuric acid (1.5 ml) was added and the mixture was heated to 75° C. while stirring for 8 h. After being left to stand overnight, the mixture was added to ice-water and stirred for 2 h. Then the precipitate was filtered off with suction and dried under high vacuum. 13.7 g of 3-pentafluorosulfanyl-5-nitrobenzoic acid were obtained.

後処理

  1. stirringthe mixture was stirred at 75° C
  2. stirringAfter stirring at 75° C. for 8 h
  3. waitthe mixture was left
  4. temperaturethe mixture was heated to 75° C.
  5. stirringwhile stirring for 8 h
  6. waitAfter being left
  7. waitto stand overnight
  8. stirringstirred for 2 h
  9. filtrationThen the precipitate was filtered off with suction
  10. customdried under high vacuum

出典と根拠

ORDレコード
ord-a6c5d621f47346a6b52aeafa8c89132e
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08198272B2

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