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

Water → 3-(Thiophen-2-yl)propan-1-ol

HRID 324774
ノート
印刷プレビュー

反応式

HRID 324774 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][CH2:7][C:8](O)=[O:9].O.C(=O)([O-])[O-].[K+].[K+]>O1CCCC1>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][CH2:7][CH2:8][OH:9]
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 962WaterHCID 11430Potassium CarbonateHCID 7031693-(2-Thienyl)propanoic acid

生成物 1

HCID 131098663-(Thiophen-2-yl)propan-1-ol収率 103.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 3-(2-thienyl)propionic acid (5.0 g, 32.0 mmol) in tetrahydrofuran (20 ml) at 0° C. was added 1 M borane tetrahydrofuran complex (33.5 ml, 33.5 mmol) dropwise over 30 minutes. The reaction mixture was then stirred for 18 h whilst warming to room temperature. The temperature was then reduced to 0° C. and water (20 ml) was added to quench the reaction. The solution was then basified with potassium carbonate, the layers separated and the aqueous layer washed with diethyl ether. The combined organic layers were washed with brine, dried and concentrated to yield the title compound (4.71 g) as an oil. DCI MS m/z 142 [M+H]+.

後処理

  1. customwas then reduced to 0° C.
  2. customto quench
  3. customthe reaction
  4. customthe layers separated
  5. washthe aqueous layer washed with diethyl ether
  6. washThe combined organic layers were washed with brine
  7. customdried
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-829ab7ee72574acab0ebff41a2be95ff
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06218538B1

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