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

Sodium Methoxide → 5-(3,4-Dimethoxyphenyl)-4,5-dihydro-1,3-oxazol-2-ol

HRID 2052558
ノート
印刷プレビュー

反応式

HRID 2052558 の反応式
C([O:3][C:4](=[O:19])[NH:5][CH2:6][CH:7]([C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[C:11]([O:17][CH3:18])[CH:10]=1)O)C.C[O-].[Na+]>C1(C)C=CC=CC=1>[CH3:18][O:17][C:11]1[CH:10]=[C:9]([CH:7]2[O:19][C:4](=[O:3])[NH:5][CH2:6]2)[CH:14]=[CH:13][C:12]=1[O:15][CH3:16]
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 2

HCID 10942334Sodium MethoxideHCID 53831097Ethyl (2-(3,4-dimethoxyphenyl)-2-hydroxyethyl)carbamate

生成物 1

HCID 30506615-(3,4-Dimethoxyphenyl)-4,5-dihydro-1,3-oxazol-2-ol収率 80%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

3 mmol of 2-(3,4-dimethoxyphenyl)-2-hydroxyethylcarbamic acid ethyl ester is suspended with 4 mmol of sodium methylate in 12 ml. of toluene and heated for 2 hours to a bath temperature of 110° under the exclusion of moisture. During this step, methanol and ethanol are distilled off. The toluene is then withdrawn under vacuum, the residue is taken up in 50 ml. of chloroform and distributed over 10 ml. of water. After drying, filtration, and concentration of the organic phase, the mixture is recrystallized from methanol, thus obtaining an 80% yield of 5-(3,4-dimethoxyphenyl)-2-oxazolidinone, m.p. 114°-117°.

後処理

  1. distillationDuring this step, methanol and ethanol are distilled off
  2. customThe toluene is then withdrawn under vacuum
  3. customAfter drying
  4. filtrationfiltration, and concentration of the organic phase
  5. customthe mixture is recrystallized from methanol

出典と根拠

ORDレコード
ord-a45e7795cf214c579e9bf74e8394bc09
出典データセット
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04186129

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