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

Methanol → Methyl(7-fluoro-6-hydroxy-4-methyl-1-benzothiophen-3-yl)acetate

HRID 591447
ノート
印刷プレビュー

反応式

HRID 591447 の反応式
[F:1][C:2]1[C:10]2[S:9][CH:8]=[C:7]([CH2:11][C:12]([OH:14])=[O:13])[C:6]=2[C:5]([CH3:15])=[CH:4][C:3]=1[OH:16].OS(O)(=O)=O.[CH3:22]O>>[CH3:22][O:13][C:12](=[O:14])[CH2:11][C:7]1[C:6]2[C:5]([CH3:15])=[CH:4][C:3]([OH:16])=[C:2]([F:1])[C:10]=2[S:9][CH:8]=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 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 89767685(7-Fluoro-6-hydroxy-4-methyl-1-benzothiophen-3-yl)acetic acid

生成物 1

HCID 121003808Methyl(7-fluoro-6-hydroxy-4-methyl-1-benzothiophen-3-yl)acetate

反応条件

温度
80 °C

実験手順

To a mixture of (7-fluoro-6-hydroxy-4-methyl-1-benzothiophen-3-yl)acetic acid (267 mg) and MeOH (8.0 mL) was added conc. H2SO4 (0.100 mL). The mixture was stirred at 80° C. for 1 h. The mixture was concentrated. The mixture was neutralized with saturated aqueous NaHCO3 and extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexane) to give the title compound (255.5 mg).

後処理

  1. concentrationThe mixture was concentrated
  2. extractionextracted with EtOAc
  3. washThe organic layer was washed with brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by silica gel column chromatography (EtOAc/hexane)

出典と根拠

ORDレコード
ord-632ff7f8bc344b4b85b28800990c4b14
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09238639B2

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