反応 #71007

反応方程式

1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone

pyridine

methoxyamine hydrochloride

→

1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oxime

収率 92.4%

溶媒

methanol

反応条件

後処理

1. 1
   その他Methanol was removed under reduced pressure
2. 2
   workup.ADDITIONthe residue poured in water (600 ml)
3. 3
   workup.ADDITION1N hydrochloric acid was added (100 ml)
4. 4
   抽出The solution was extracted with dichloromethane (3×300 ml)
5. 5
   洗浄Combined organic layers were washed with brine (500 ml)
6. 6
   乾燥dried over sodium sulfate
7. 7
   その他The solvent was removed in vacuo

実験手順

To a stirred solution of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone (162 g; 0.97 mol), prepared as described in example P4, in methanol (500 ml) was added pyridine (160 ml; 1.95 mol) followed by a portionwise addition of methoxyamine hydrochloride (142 g; 1.70 mol). The reaction mixture was stirred at 24° C. for 16 hours under nitrogen atmosphere. Methanol was removed under reduced pressure, the residue poured in water (600 ml) and 1N hydrochloric acid was added (100 ml). The solution was extracted with dichloromethane (3×300 ml). Combined organic layers were washed with brine (500 ml) and dried over sodium sulfate. The solvent was removed in vacuo to afford 175 g (92% of theory) of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oxime as a clear red oil.

出典