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

Potassium Carbonate → 1-Methyl-5-[3-(2-naphthoyl)propyl]thio-1,2,3,4-tetrazole

HRID 1758307
ノート
印刷プレビュー

反応式

HRID 1758307 の反応式
[CH3:1][N:2]1[C:6]([SH:7])=[N:5][N:4]=[N:3]1.C(=O)([O-])[O-].[K+].[K+].[CH:14]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=[CH:16][C:15]=1[C:24]([CH2:26][CH2:27][CH2:28]Cl)=[O:25]>CC(C)=O>[CH3:1][N:2]1[C:6]([S:7][CH2:28][CH2:27][CH2:26][C:24]([C:15]2[CH:16]=[CH:17][C:18]3[C:23](=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH:14]=2)=[O:25])=[N:5][N:4]=[N:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 122875592-(4-Chlorobutyryl)naphthaleneHCID 178482017HCID 178482017、化合物

生成物 1

HCID 130916401-Methyl-5-[3-(2-naphthoyl)propyl]thio-1,2,3,4-tetrazole収率 51%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

1-Methyl-5-mercapto-1,2,3,4-tetrazole (1.2 g), potassium carbonate (2.1 g) and 3-chloropropyl 2-naphthyl ketone (3.5 g) are added to acetone (50 ml) and the mixture is refluxed with stirring for 2 hours. The reaction mixture is concentrated to dryness under reduced pressure and the residue dissolved in chloroform. Insolubles are filtered off. The filtrated is concentrated and the residue is purified by silica gel column chromatography [Kieselgel 60, eluant: benzene-ether (10:1)] and the product is recrystallized from ethanol to obtain 1-methyl-5-[3-(2-naphthoyl)propyl]thio-1,2,3,4-tetrazole (yield 51%) as colorless prisms, m.p. 118°-120° C.

後処理

  1. temperaturethe mixture is refluxed
  2. concentrationThe reaction mixture is concentrated to dryness under reduced pressure
  3. dissolutionthe residue dissolved in chloroform
  4. filtrationInsolubles are filtered off
  5. concentrationThe filtrated is concentrated
  6. customthe residue is purified by silica gel column chromatography [Kieselgel 60, eluant: benzene-ether (10:1)]
  7. customthe product is recrystallized from ethanol

出典と根拠

ORDレコード
ord-3c70934276be439686996f6975bd570f
出典データセット
uspto-grants-1983_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04372953

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