Hydrochloric Acid → HCID 86733541、化合物
反応式
C1(C)C=CC(S(Cl)(=O)=O)=CC=1.[OH:12][CH2:13][CH2:14]/[CH:15]=[CH:16]\[CH2:17][C:18]([O:20][CH:21]([CH3:23])[CH3:22])=[O:19].Cl.C(=O)([O-])[O-].[Na+].[Na+].[S:31]([C:35]1[CH:41]=[CH:40][C:38]([CH3:39])=[CH:37][CH:36]=1)([O-:34])(=[O:33])=[O:32]>N1C=CC=CC=1>[C:38]1([CH3:39])[CH:37]=[CH:36][C:35]([S:31]([OH:34])(=[O:32])=[O:33])=[CH:41][CH:40]=1.[OH:12][CH2:13][CH2:14]/[CH:15]=[CH:16]\[CH2:17][C:18]([O:20][CH:21]([CH3:23])[CH3:22])=[O:19]参加物
7
反応条件
- 温度
- 0 °C
実験手順
p-Toluene sulfonyl chloride (1.425 g., 7.5 mm.) was added at 0°C to a solution of 1.00 g. (5.8 mm.) of isopropyl cis 6-hydroxy-3-hexenoate in 2.37 g. of dry pyridine. The resulting mixture was stirred at 0°C for 4 hours. The crude product was poured on ice and concentrated hydrochloric acid, sodium carbonate till neutral and dried over potassium carbonate. Evaporation of the solvent produced 1.32 g. (70% of theory) of crude tosylate.
後処理
- dry with materialdried over potassium carbonate
- customEvaporation of the solvent
- customproduced 1.32 g
出典と根拠
- ORDレコード
- ord-3ce3ea93aefa46e29e39db5cfa09756f
- 出典データセット
- uspto-grants-1976_06
- 特許番号
- US03962354
反応ノート
読み込み中…