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 → Sodium 4-(2-methanesulfonyl-4-methoxycarbonyl-5-methylphenoxy)-2-pentafluorosulfanylbenzenesulfinate

HRID 269419
ノート
印刷プレビュー

反応式

HRID 269419 の反応式
Cl[S:2]([C:5]1[CH:26]=[CH:25][C:8]([O:9][C:10]2[C:19]([S:20]([CH3:23])(=[O:22])=[O:21])=[CH:18][C:13]([C:14]([O:16][CH3:17])=[O:15])=[C:12]([CH3:24])[CH:11]=2)=[CH:7][C:6]=1[S:27]([F:32])([F:31])([F:30])([F:29])[F:28])(=[O:4])=[O:3].[O-]S([O-])=O.[Na+:37].[Na+].[OH-].[Na+].Cl>O>[CH3:23][S:20]([C:19]1[CH:18]=[C:13]([C:14]([O:16][CH3:17])=[O:15])[C:12]([CH3:24])=[CH:11][C:10]=1[O:9][C:8]1[CH:25]=[CH:26][C:5]([S:2]([O-:4])=[O:3])=[C:6]([S:27]([F:28])([F:29])([F:30])([F:32])[F:31])[CH:7]=1)(=[O:21])=[O:22].[Na+:37]
参加物反応条件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 14798Sodium HydroxideHCID 24437Sodium SulfiteHCID 59832570Methyl 4-(4-chlorosulfonyl-3-pentafluorosulfanylphenoxy)-5-methanesulfonyl-2-methylbenzoate

生成物 1

HCID 86616338Sodium 4-(2-methanesulfonyl-4-methoxycarbonyl-5-methylphenoxy)-2-pentafluorosulfanylbenzenesulfinate

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
70 °C

実験手順

3.5 g of methyl 4-(4-chlorosulfonyl-3-pentafluorosulfanylphenoxy)-5-methanesulfonyl-2-methylbenzoate were added in portions to a solution of 8.10 g of Na2SO3 in 75 ml of water at 70° C., during which the pH was kept at about pH=10 with 10 molar aqueous NaOH solution. The mixture is then stirred at 70° C. for 45 minutes and, after being allowed to cool, the pH is adjusted to pH=2 with aqueous HCl solution. 3 extractions with 200 ml of EA each time were carried out. After drying over MgSO4, the solvent was removed in vacuo. The residue was suspended in 100 ml of water and adjusted to pH=10 with a 2 molar aqueous NaOH solution, and the volatiles were removed in vacuo. Coevaporation was then carried out firstly twice with 100 ml of toluene each time and then with 100 ml of anhydrous DMF, and the residue (3.0 g) was reacted further without purification.

後処理

  1. temperatureto cool
  2. extraction3 extractions with 200 ml of EA each time
  3. dry with materialAfter drying over MgSO4
  4. customthe solvent was removed in vacuo
  5. customthe volatiles were removed in vacuo
  6. customwith 100 ml of anhydrous DMF, and the residue (3.0 g) was reacted further without purification

出典と根拠

ORDレコード
ord-d96878f9ff6e4f128b7a34ff48cf1526
出典データセット
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07446225B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート