反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- -73 °C
PROCEDURE
实验过程
tert-Butyl (3-oxocyclobutyl)carbamate (43.2 g, 233 mmol) was charged into a 2 L 3-necked flask equipped with a thermometer and an addition funnel. THF (0.7 L) was added and the mixture was cooled to −73° C. internal temperature. Lithium borohydride, 2M in THF (140 mL, 280 mmol) was added over 30 minutes via the addition funnel, during which time the temperature did not exceed −72° C. After stirring for an additional 1 h at that temperature, TLC analysis indicated reaction was complete. Saturated aqueous ammonium chloride (0.3 L) was added and the mixture was warmed to 0° C. After gas evolution ceased, EtOAc (0.3 L) and water (0.3 L) were added and the mixture was stirred vigorously for 1 h. The layers were then separated and the aqueous layer was extracted with EtOAc (1×). The combined extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to give a yellow solid. This solid was suspended in 3:1 EtOAc/hexane and heated to boiling. The remaining solid was filtered off and additional hexane (100 mL) was added to the filtrate. The filtrate was then cooled in the freezer overnight. The resulting solid was collected by filtration and washed with cold 1:1 EtOAc/hexane solution, then dried to give tert-butyl(cis-3-hydroxycyclobutyl)carbamate (25.8 g, 59.0% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.36 (s, 9 H) 1.68 (qd, J=8.54, 2.93 Hz, 2 H) 2.33-2.45 (m, 2 H) 3.34-3.44 (m, 1 H) 3.65-3.76 (m, 1 H) 4.98 (d, J=5.67 Hz, 1 H) 7.03 (d, J=7.82 Hz, 1 H).
WORKUP
后处理
- customequipped with a thermometer and an addition funnel
- customdid not exceed −72° C
- customreaction
- temperaturethe mixture was warmed to 0° C
- stirringthe mixture was stirred vigorously for 1 h
- customThe layers were then separated
- extractionthe aqueous layer was extracted with EtOAc (1×)
- dry with materialThe combined extracts were dried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto give a yellow solid
- temperatureheated to boiling
- filtrationThe remaining solid was filtered off
- additionadditional hexane (100 mL) was added to the filtrate
- temperatureThe filtrate was then cooled in the freezer overnight
- filtrationThe resulting solid was collected by filtration
- washwashed with cold 1:1 EtOAc/hexane solution
- customdried