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

2,5-Dimethoxytetrahydrofuran → 2-Sulfo-2-(1-pyrryl)acetic acid

HRID 26316
ノート
印刷プレビュー

反応式

HRID 26316 の反応式
C([O-])(=O)C.[Na+].Cl.[S:7]([CH:11]([NH2:15])[C:12]([OH:14])=[O:13])([OH:10])(=[O:9])=[O:8].CO[CH:18]1[CH2:22][CH2:21][CH:20](OC)O1>C(O)(=O)C.C(OC(=O)C)C>[S:7]([CH:11]([N:15]1[CH:18]=[CH:22][CH:21]=[CH:20]1)[C:12]([OH:14])=[O:13])([OH:10])(=[O:9])=[O:8]
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 3

HCID 790982,5-DimethoxytetrahydrofuranHCID 517045Sodium AcetateHCID 86736466alpha-Sulfo-alpha-aminoacetic acid hydrochloride

生成物 1

HCID 867364652-Sulfo-2-(1-pyrryl)acetic acid

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒2 回HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of sodium acetate (0.1 mole) in about 300 ml of glacial acetic acid is added about 0.05 mole of α-sulfo-α-aminoacetic acid hydrochloride. The solution is heated to reflux for 5 minutes, 2,5-dimethoxytetrahydrofuran (1 equivalent based on α-sulfo-α-aminoacetic acid hydrochloride) is added as quickly as possible, and the solution refluxed for an additional 2 minutes. The acetic acid is flash evaporated leaving a residue which is taken up in ethylacetate. The ethyl acetate is filtered, dried and evaporated to give α-sulfo-α-(1-pyrryl) acetic acid.

後処理

  1. temperatureThe solution is heated
  2. temperatureto reflux for 5 minutes
  3. temperaturerefluxed for an additional 2 minutes
  4. customevaporated
  5. customleaving a residue which
  6. filtrationThe ethyl acetate is filtered
  7. customdried
  8. customevaporated

出典と根拠

ORDレコード
ord-6e1284b316994e4b8f3c00440d36aaba
出典データセット
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04148998

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