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

Trifluoroacetic acid → 7-(2-Thienylacetamido)-3-(1-acetoxyethyl)-3-cephem-4-carboxylic acid

HRID 596837
ノート
印刷プレビュー

反応式

HRID 596837 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][C:7]([NH:9][CH:10]1[C:39](=[O:40])[N:12]2[C:13]([C:23]([O:25]C(C3C=CC=CC=3)C3C=CC=CC=3)=[O:24])=[C:14]([CH:17]([O:19][C:20](=[O:22])[CH3:21])[CH3:18])[CH2:15][S:16][C@H:11]12)=[O:8].C1(OC)C=CC=CC=1.FC(F)(F)C(O)=O.CCCCCCC>CC(C)=O>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][C:7]([NH:9][CH:10]1[C:39](=[O:40])[N:12]2[C:13]([C:23]([OH:25])=[O:24])=[C:14]([CH:17]([O:19][C:20](=[O:22])[CH3:21])[CH3:18])[CH2:15][S:16][C@H:11]12)=[O:8]
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

6

反応物 4

HCID 6422Trifluoroacetic acidHCID 7519AnisoleHCID 8900HeptaneHCID 70617769Diphenylmethyl 7-(2-thienylacetamido)-3-(1-acetoxyethyl)-3-cephem-4-carboxylate

生成物 1

HCID 706176497-(2-Thienylacetamido)-3-(1-acetoxyethyl)-3-cephem-4-carboxylic acid収率 40.5%

試薬・触媒・溶媒 1

HCID 180
Acetone
溶媒

反応条件

温度
5 °C

実験手順

To a cooled (5° C.), stirred solution of 0.328 g. of benzhydryl 7-(2-thienylacetamido)-3-(1-acetoxyethyl)-3-cephem-4-carboxylate in 1 ml. of anisole was added 1 ml. of cold trifluoroacetic acid. The reaction mixture was allowed to stir with cooling for 20 minutes after which time was added 30 ml. of n-heptane. The reaction mixture was evaporated in vacuo to a low volume, 20 ml. of n-heptane was added, and the resulting mixture was stirred with cooling for five minutes. The solid obtained by filtration of the resulting solution was dissolved in acetone, and the acetone solution was then filtered and evaporated to near dryness. The residue was dissolved in ethyl acetate, and the resulting solution was extracted three times with cold aqueous sodium bicarbonate solution. The aqueous extracts were combined, layered with ethyl acetate, and acidified with 1N.HCl. The organic layer was separated, washed with brine, and dried over anhydrous sodium sulfate. Evaporation in vacuo to dryness gave 94 mg. (40.5 percent) of the title product:

後処理

  1. stirringto stir
  2. temperaturewith cooling for 20 minutes after which time
  3. additionwas added 30 ml
  4. customThe reaction mixture was evaporated in vacuo to a low volume, 20 ml
  5. additionof n-heptane was added
  6. stirringthe resulting mixture was stirred
  7. temperaturewith cooling for five minutes
  8. customThe solid obtained by filtration of the resulting solution
  9. filtrationthe acetone solution was then filtered
  10. customevaporated
  11. dissolutionThe residue was dissolved in ethyl acetate
  12. extractionthe resulting solution was extracted three times with cold aqueous sodium bicarbonate solution
  13. customThe organic layer was separated
  14. washwashed with brine
  15. dry with materialdried over anhydrous sodium sulfate
  16. customEvaporation in vacuo to dryness
  17. customgave 94 mg

出典と根拠

ORDレコード
ord-0a26186a70b3485a9d971caa6bd878d0
出典データセット
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04012380

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