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Cis-4-thiocyano-3-buten-2-one → HCID 178467920、化合物

HRID 1463791
ノート
印刷プレビュー

反応式

HRID 1463791 の反応式
O.[Na].[SH:3][C:4]1[N:8]([CH3:9])[N:7]=[N:6][N:5]=1.S(/[CH:13]=[CH:14]\[C:15](=[O:17])[CH3:16])C#N>C(O)C>[SH:3][C:4]1[N:8]([CH3:9])[N:7](/[CH:13]=[CH:14]\[C:15](=[O:17])[CH3:16])[NH:6][N:5]=1
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

4

反応物 2

HCID 45085240Cis-4-thiocyano-3-buten-2-one2 回HCID 178482031HCID 178482031、化合物

生成物 1

HCID 178467920HCID 178467920、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

反応条件

温度
25 °C

実験手順

To a stirred solution of 5-mercapto-1-methyltetrazole sodium salt hydrate (1.1 g., 0.008 mole) in aqueous ethanol (15 ml), a solution of cis-4-thiocyano-3-buten-2-one (Compound 28) in ethanol was added dropwise over 5 minutes. A solid suspension was observed forming over the next 2 hours which was stirred at 25° C. for 18 hours. The volatiles were removed in vacuo and the residue was extracted into ethyl acetate and washed thoroughly with water. After drying (MgSO4), the solution was concentrated. The solid residue was purified via column chromatography on silica gel using hexanes/ethyl acetate (3:2) as eluant to yield 1.1 g of a white solid, mp 112°-114° C. IR (nujol) uc=o 1660 cm-1.

後処理

  1. customA solid suspension was observed forming over the next 2 hours which
  2. customThe volatiles were removed in vacuo
  3. extractionthe residue was extracted into ethyl acetate
  4. washwashed thoroughly with water
  5. dry with materialAfter drying (MgSO4)
  6. concentrationthe solution was concentrated
  7. customThe solid residue was purified via column chromatography on silica gel

出典と根拠

ORDレコード
ord-ed9be222d7c344df9a075c8e40d5a5bb
出典データセット
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05302592

反応ノート

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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