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

Chloromethyl Methyl Ether → HCID 131719456、化合物

HRID 1734507
ノート
印刷プレビュー

反応式

HRID 1734507 の反応式
[OH:1][CH2:2][C@@H:3]1[CH2:7][S:6][C:5]([S:8][CH3:9])=[N:4]1.[CH:10](N(C(C)C)CC)(C)C.Cl[CH2:20][O:21]C>ClCCl>[CH3:20][O:21][C@:3]1([CH2:2][O:1][CH3:10])[CH2:7][S:6][C:5]([S:8][CH3:9])=[N:4]1
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 7864Chloromethyl Methyl EtherHCID 81531DiisopropylethylamineHCID 22862349(4R)-4,5-Dihydro-2-(methylthio)-4-thiazolemethanol

生成物 1

HCID 131719456HCID 131719456、化合物収率 36%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

3.14 g of Compound (6) obtained in the step (a) and 6.7 ml of diisopropylethylamine were dissolved in 40 ml of dry dichloromethane solution. 2.33 g of chloromethylmethyl ether was added to the above mixture under ice-cooling and the reaction mixture was stirred for 1 hour under the same condition and for 15 hours at room temperature. After the reaction, the reaction mixture was washed with water, saturated sodium bicarbonate solution and saturated saline solution, and dried over magnesium sulfate. After removal of the solvent, the resulting residue was purified by silica gel column chromatography (chloroform-ethyl acetate) to give 1.42 g (36%) of 4(R)-methoxy-methyloxymethyl-2-methylthio-1,3-thiazoline [Compound (7)].

後処理

  1. temperaturecooling
  2. customAfter the reaction
  3. washthe reaction mixture was washed with water, saturated sodium bicarbonate solution and saturated saline solution
  4. dry with materialdried over magnesium sulfate
  5. customAfter removal of the solvent
  6. customthe resulting residue was purified by silica gel column chromatography (chloroform-ethyl acetate)

出典と根拠

ORDレコード
ord-cdc12c897c9249a9b32294e176cb2c1d
出典データセット
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05534510

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