反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- -4 °C
PROCEDURE
实验过程
A round-bottom flask was charged with lithium aluminum hydride (3.5 g, 88 mmol), and the flask was placed in an brine/ice bath. Tetrahydrofuran (100 mL) was added slowly. The resulting solution was maintained at −4° C. with stirring. A solution of 4-benzyloxy-6-fluoro-3-methyl-naphthalene-2-carboxylic acid methyl ester (14.27 g, 44.00 mmol) in tetrahydrofuran (30 mL) was slowly added to the cold lithium aluminum hydride suspension drop-wise via an addition funnel. The rate of drop-wise addition was monitored so that the reaction temperature did not exceed 6° C. After the drop-wise addition was complete, the reaction was warmed to room temperature. The reaction mixture was stirred at room temperature for 1 hour. After this time, the reaction mixture was cooled to 4° C. in an ice bath. Water (3.5 mL) was added slowly, keeping the reaction temperature below 4° C. A 15% aqueous NaOH solution (3.5 mL) was next added, followed by an additional portion of water (10.5 mL). The precipitated solids were filtered, and then rinsed with ethyl acetate. The combined filtrates were concentrated to obtain 13.09 g (quantitative yield) of (4-benzyloxy-6-fluoro-3-methyl-naphthalen-2-yl)-methanol as a white solid. This product was used in the next step without additional purification. 1H NMR (300 MHz, DMSO-d6) δ ppm 8.00 (dd, J=8.9, 5.9 Hz, 1 H), 7.77 (s, 1 H), 7.54-7.63 (m, 3 H), 7.31-7.51 (m, 4 H), 5.26-5.35 (m, 1 H), 4.94 (s, 2 H), 4.64 (d, J=5.1 Hz, 2 H), 2.34 (s, 3 H).
WORKUP
后处理
- customthe flask was placed in an brine/ice bath
- additionThe rate of drop-wise addition
- customdid not exceed 6° C
- additionAfter the drop-wise addition
- temperaturethe reaction was warmed to room temperature
- stirringThe reaction mixture was stirred at room temperature for 1 hour
- temperatureAfter this time, the reaction mixture was cooled to 4° C. in an ice bath
- customthe reaction temperature below 4° C
- filtrationThe precipitated solids were filtered
- washrinsed with ethyl acetate
- concentrationThe combined filtrates were concentrated