Bromoacetic Acid → HCID 22220817、化合物
反応式
[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:6]([OH:8])[CH3:7].Br[CH2:10][C:11]([OH:13])=[O:12]>O>[C:11]([CH2:10][N:3]1[CH:4]=[CH:5][S:1][CH:2]1[CH:6]([OH:8])[CH3:7])([OH:13])=[O:12]参加物
4
実験手順
1-(2-Thiazolyl)ethanol (0.5 g, 3.87 mmole) and bromoacetic acid (0.538 g, 3.87 mmole) were warmed to melt the bromoacetic acid, then were allowed to cool and were stirred 4 days at room temp. The mixture was dissolved in 15–20 mL water and extracted with 4×10 mL ether. The water layer was evaporated in vacuo to give 0.79 g of residue, which was stored under 30 mL acetonitrile at room temp. overnight to effect crystalization. Filtration and washing with 30% ether/acetonitrile gave 0.335 g of the title compound, mp 160–161 C.
後処理
- temperatureto cool
- extractionextracted with 4×10 mL ether
- customThe water layer was evaporated in vacuo
出典と根拠
- ORDレコード
- ord-b2dfab04c77c4ca6bc79b9876a99a97d
- 出典データセット
- uspto-grants-2006_04
- 特許番号
- US07022721B1
反応ノート
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