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
- 60 °C
PROCEDURE
实验过程
4-(3,3-dimethyl-cyclobutanecarbonyl)-benzoic acid ethyl ester (Intermediate 23) (235 mg, 0.903 mmol) was dissolved in methanol (5 mL). Ammonium acetate (710 mg, 9.03 mmol) was added followed by sodium cyanoborohydride (89.6 mg, 1.36 mmol). This was heated to 60° C. for 17 h before cooling and adding 1 N HCl (3 mL). This was stirred for 15 min and then 1N NaOH (10 mL) was added. The material was extracted into two portions of ethyl acetate and the combined organics dried over MgSO4. Purification by silica gel flash chromatography (methanol/ethyl acetate) gave (+/−)-4-[amino-(3,3-dimethyl-cyclobutyl)-methyl]-benzoic acid ethyl ester (137 mg) as a pale yellow oil. 1H NMR (400 MHz, CDCl3) δ 7.99 (d, J=8.4 Hz, 2 H) 7.37 (d, J=8.2 Hz, 2 H) 4.38 (q, J=7.0 Hz, 2 H) 3.82 (d, J=9.2 Hz, 1H) 2.39 (sxt, J=8.7 Hz, 1 H) 1.90-2.02 (m, 1 H) 1.60-1.70 (m, 1 H) 1.46-1.57 (m, 2 H) 1.40 (t, J=7.1 Hz, 3 H) 1.11 (s, 3 H) 1.06 (s, 3H); GCMS (M): 261.
WORKUP
后处理
- temperaturebefore cooling
- extractionThe material was extracted into two portions of ethyl acetate
- dry with materialthe combined organics dried over MgSO4
- customPurification by silica gel flash chromatography (methanol/ethyl acetate)