反応式
[SH:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4][OH:5].S[CH:11]([OH:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.Cl.[CH2:20](N(CC)CC)[CH3:21]>COCCOCCOC>[CH2:20]([C:12]([CH2:13][S:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4][OH:5])([CH:17]=[CH:16][CH2:15][CH3:14])[CH:11]=[O:18])[CH3:21]参加物
6
実験手順
A mixture of 5.0 g (0.036 mole) of 2-mercaptobenzyl alcohol, 6.4 g (0.032 mole) of 1, 3.6 g (0.036 mole) of triethylamine and 25 mL of 2-methoxyethyl ether was held at reflux for 7 h. Additional 1.1 g of mercaptobenzyl alcohol and 0.72 g of triethylamine was added to the reaction mixture and the mixture was held at reflux for additional 16 h. The reaction mixture was cooled and poured into 6N HCl and extracted with methylene chloride. The methylene chloride extract was wasted twice with 10% NaOH, dried over MgSO4 and concentrated in vacto to give 9.6 g of residue. Purification by HPLC (20% EtOAc-hexane) gave 3.7 g (41%) of 16 as an oil.
後処理
- temperatureat reflux for 7 h
- temperatureat reflux for additional 16 h
- temperatureThe reaction mixture was cooled
- extractionextracted with methylene chloride
- extractionThe methylene chloride extract
- dry with materialdried over MgSO4
- concentrationconcentrated in vacto
出典と根拠
- ORDレコード
- ord-346d294e4065472690ba939724fcfb29
- 出典データセット
- uspto-grants-2005_09
- 特許番号
- US06943189B2
関連ノート
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