反応 #58791

反応方程式

compound ( 6 )

Benzyl 1-Aminomethyl-1-Cyclohexane Acetate Hydrochloride

1-chloroethyl chloroformate

N-methylmorpholine

→

title compound ( 9 )

収率 100.6%

Benzyl 1-{[(α-Chloroethoxy)carbonyl]aminomethyl}-1-Cyclohexane Acetate

収率 100.6%

溶媒

dichloromethane

反応条件

後処理

1. 1
   温度with cooling, over a one hour period
2. 2
   workup.STIRRINGThe resulting turbid solution was stirred for 30 min
3. 3
   その他the reaction
4. 4
   洗浄The reaction mixture was washed with water (2×2 L) and brine (1 L)
5. 5
   乾燥dried over sodium sulfate
6. 6
   その他Evaporation of the solvent

実験手順

In a 5-liter, 3-neck, round bottom flask, stirred mechanically and under nitrogen, was added dichloromethane (1.5 L), compound (6) (1.85 mol) and 1-chloroethyl chloroformate (258 g, 1.81 mol). The resulting solution was cooled to 15° C. and N-methylmorpholine (396 mL, 3.60 mol) was added slowly, with cooling, over a one hour period. The resulting turbid solution was stirred for 30 min, after which 1H—NMR analysis showed the reaction to be complete. The reaction mixture was washed with water (2×2 L) and brine (1 L) and dried over sodium sulfate. Evaporation of the solvent afforded the title compound (9) as an orange oil (670 g, 98% yield). 1HNMR (CDCl3, 400 MHz): 1.33-1.53 (m, 10H), 1.75 (d, 3H), 2.33 (s, 2H), 3.18 (d, 2H), 5.09 (s, 2H), 5.58 (t, 1H), 6.53 (q, 1H), 7.29-7.33 (m, 5H).

出典