Acetyl chloride → Methyl 7-hydroxyhept-5-ynoate
反応式
C([O:4][CH2:5][C:6]#[C:7][CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])(=O)C.[C:14](Cl)(=O)C.C(=O)(O)[O-].[Na+]>CO>[CH3:14][O:13][C:11](=[O:12])[CH2:10][CH2:9][CH2:8][C:7]#[C:6][CH2:5][OH:4]参加物
5
実験手順
The crude acid 29 (6.333 g) was treated with a 1% solution of acetyl chloride in methanol (60 mL). After 16 h, sodium bicarbonate (1.966 g, 23.4 mmol) was added. The mixture was dried (MgSO4), filtered through celite and evaporated in vacuo. Purification by flash chromatography on silica gel (30-40% ethyl acetate/hexanes) gave 7-Hydroxy-hept-5-ynoic acid methyl ester 30 (3.022 g, 19.3 mmol, 92% from 7-(tert-Butyl-dimethyl-silanyloxy)-hept-2-yn-1-ol 27).
後処理
- dry with materialThe mixture was dried (MgSO4)
- filtrationfiltered through celite
- customevaporated in vacuo
- customPurification by flash chromatography on silica gel (30-40% ethyl acetate/hexanes)
出典と根拠
- ORDレコード
- ord-0c00cfeee375472f841eceb70c1b5530
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08754122B2
反応ノート
読み込み中…