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 → HCID 54569995、化合物

HRID 257330
ノート
印刷プレビュー

反応式

HRID 257330 の反応式
[C:1]([O:4][C:5](=O)[CH3:6])(=[O:3])[CH3:2].S(=O)(=O)(O)O.[CH3:13][O:14][C:15]([C:17]1([F:23])CC[CH2:19][CH:18]1O)=[O:16]>>[CH3:13][O:14][C:15]([C:17]1([F:23])[CH2:18][CH2:19][CH2:6][CH:5]1[O:4][C:1](=[O:3])[CH3:2])=[O:16]
参加物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 1118Sulfuric AcidHCID 7918Acetic AnhydrideHCID 19783080HCID 19783080、化合物

生成物 1

HCID 54569995HCID 54569995、化合物収率 73.5%

実験手順

0.32 g (3 mmol) of acetic anhydride and a catalytic amount of concentrated sulfuric acid were added at room temperature to 0.5 g (3 mmol) of 1-fluoro-2-hydroxycyclopentanecarboxylic acid methyl ester in cis form (compound number 2a) synthesized in Example 1, and the mixture was stirred for 5 hours. The reaction solution was poured into ice water and extracted with ethyl acetate, and the extract was successively washed with saturated saline, a saturated aqueous sodium bicarbonate solution and saturated saline. The ethyl acetate layer was dried over anhydrous magnesium sulfate and the solvent was distilled away to obtain 0.45 g (yield: 72%) of the objective 2-acetoxy-1-fluoro-1-cyclopentanecarboxylic acid methyl ester in cis form (compound number 3a).

後処理

  1. customsynthesized in Example 1
  2. extractionextracted with ethyl acetate
  3. washthe extract was successively washed with saturated saline
  4. dry with materialThe ethyl acetate layer was dried over anhydrous magnesium sulfate
  5. distillationthe solvent was distilled away

出典と根拠

ORDレコード
ord-be02a21cd978486d86de4bdc35b9eabb
出典データセット
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05262385

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