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

Diethyl Ether → Benzyl (2s)-2-[(4-cyanophenoxy)methyl]-1-aziridinecarboxylate

HRID 411543
ノート
印刷プレビュー

反応式

HRID 411543 の反応式
[OH-].[Na+].CS(O[C@@H:8]([CH2:21][O:22][C:23]1[CH:28]=[CH:27][C:26]([C:29]#[N:30])=[CH:25][CH:24]=1)[CH2:9][NH:10][C:11]([O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:12])(=O)=O.CCOCC>O.S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.C(Cl)Cl>[C:29]([C:26]1[CH:27]=[CH:28][C:23]([O:22][CH2:21][C@@H:8]2[CH2:9][N:10]2[C:11]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:12])=[CH:24][CH:25]=1)#[N:30]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 3283Diethyl EtherHCID 14798Sodium HydroxideHCID 88118165(1R)-2-{[(Benzyloxy)carbonyl]amino}-1-[(4-cyanophenoxy)methyl]ethyl Methanesulfonate

生成物 1

HCID 90843497Benzyl (2s)-2-[(4-cyanophenoxy)methyl]-1-aziridinecarboxylate収率 69%

試薬・触媒・溶媒 3

HCID 94433Tetrabutylammonium hydrogen sulfate触媒
HCID 962
Water
溶媒
2 回
HCID 6344Dichloromethane溶媒

実験手順

A solution of NaOH in water (11 mL of 50 wt. %) was added under vigorous stirring to a solution of (1R)-2-{[(benzyloxy)carbonyl]amino}-1-[(4-cyanophenoxy)-methyl]ethyl methanesulfonate (see step (iv) above; 5.7 g, 14.1 mmol) and tetrabutylammonium hydrogensulfate (0.6 g, 1.7 mmol) in DCM (34 mL). The mixture was stirred for 1 h before water (200 mL) and ether (200 mL) were added. The organic phase was washed with water and then dried. The solvents were evaporated and the resulting residue was purified by chromatography (DCM eluant) to yield 3.0 g (69%) of the sub-title compound.

後処理

  1. additionwere added
  2. washThe organic phase was washed with water
  3. customdried
  4. customThe solvents were evaporated
  5. customthe resulting residue was purified by chromatography (DCM eluant)

出典と根拠

ORDレコード
ord-43e786769e104bee825856b26c727f52
出典データセット
uspto-grants-2003_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06559162B2

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