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 → N-(Phenylsulfonyl)-tetrahydro-2-nitromethylene-2H-1,3-thiazine

HRID 371347
ノート
印刷プレビュー

反応式

HRID 371347 の反応式
CC(C)([O-])C.[K+].[SH:7][CH2:8][CH2:9][CH2:10][NH:11][S:12]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)(=[O:14])=[O:13].Cl[C:22](Cl)=[CH:23][N+:24]([O-:26])=[O:25].Cl.[Cl-].[Na+]>C(O)(C)(C)C>[C:15]1([S:12]([N:11]2[CH2:10][CH2:9][CH2:8][S:7][C:22]2=[CH:23][N+:24]([O-:26])=[O:25])(=[O:14])=[O:13])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 5234Sodium ChlorideHCID 122195711,1-Dichloro-2-nitroetheneHCID 20238482N-(3-Mercaptopropyl)benzenesulfonamideHCID 23665647Potassium tert-butoxide

生成物 1

HCID 53713608N-(Phenylsulfonyl)-tetrahydro-2-nitromethylene-2H-1,3-thiazine

試薬・触媒・溶媒 1

HCID 6386tert-Butanol溶媒

実験手順

0.22 g of potassium t-butoxide was added drop-by-drop over 10 minutes to a solution of 0.23 g of 3 in 5 ml of t-butanol, under nitrogen. The resulting mixture was added drop-by-drop over 20 minutes to 0.30 g of 13A. After 20 minutes at room temperature, the mixture was poured into 2% hydrochloric acid saturated with sodium chloride, the resulting mixture was extracted with methylene chloride, the solvent was evaporated from the extract and the residue was purified over silica gel, using methylene chloride as eluent, to give 25, m.p: 106°-107° C.

後処理

  1. extractionthe resulting mixture was extracted with methylene chloride
  2. customthe solvent was evaporated from the
  3. extractionextract
  4. customthe residue was purified over silica gel

出典と根拠

ORDレコード
ord-aa261ecb44a94b3ca6b1d920bea0bfc3
出典データセット
uspto-grants-1985_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04531002

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