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

Sulfuric Acid → Methyl 4-amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylate

HRID 1459458
ノート
印刷プレビュー

反応式

HRID 1459458 の反応式
S(=O)(=O)(O)O.[NH2:6][C:7]1[C:12]2[CH2:13][CH2:14][O:15][C:11]=2[C:10]([C:16]([OH:18])=[O:17])=[CH:9][C:8]=1[Cl:19].[CH3:20]O.N>CO>[NH2:6][C:7]1[C:12]2[CH2:13][CH2:14][O:15][C:11]=2[C:10]([C:16]([O:18][CH3:20])=[O:17])=[CH:9][C:8]=1[Cl:19]
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 1118Sulfuric AcidHCID 106324014-Amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylic acidHCID 21705897Ammonia methanol

生成物 1

HCID 54393661Methyl 4-amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylate収率 81%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Sulfuric acid (18 ml) was added dropwise to cooled methanol (90 ml). 4-Amino-5-chloro-2,3-dihydro-7-benzofurancarboxylic acid (20 g) was added to the mixture which was subsequently stirred and refluxed for 3 hours. The reaction mixture was cooled and alkalized with CH3OH/NH3. The solvent was evaporated and the residue stirred in water. The precipitate was filtered off and washed with water and DIPE. The remaining solid was dried, yielding 17.2 g (81%) of methyl 4-amino-5-chloro-2,3-di-hydro-7-benzofurancarboxylate (intermediate 1; mp. 135.4° C.).

後処理

  1. temperaturerefluxed for 3 hours
  2. temperatureThe reaction mixture was cooled
  3. customThe solvent was evaporated
  4. stirringthe residue stirred in water
  5. filtrationThe precipitate was filtered off
  6. washwashed with water and DIPE
  7. customThe remaining solid was dried

出典と根拠

ORDレコード
ord-d314552f3561435091baf9e2e889820b
出典データセット
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05854261

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