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
PROCEDURE
实验过程
The toluene solution from Step 1 was cooled in an ice bath under N2 and triflic acid (9.44 L) added slowly over 3 h. On stirring a fine white solid was formed which dissolved on warming to RT over 20 h and then stirring at RT for 37 h to give a yellow solution. To the solution was added acetyl chloride (726 mL) and the solution stirred at RT for a further 1 h. This solution was cannulated into a stirred cooled (0° C.) solution of EtOAc (217.8 L) and NaOAc.3H2O (14.52 Kg) dissolved in water (145 L). The organic phase was washed with saturated brine (twice, 72.6 L), and was evaporated to 5.5 Kg. Toluene:Isopropanol (2:3) was added and the crystalline solid removed by filtration and dried to give 12.6 Kg (61% over 2 steps), mp 124-126° C.
WORKUP
后处理
- customwas formed which
- dissolutiondissolved
- stirringstirring at RT for 37 h
- customto give a yellow solution
- stirringthe solution stirred at RT for a further 1 h
- washThe organic phase was washed with saturated brine (twice, 72.6 L), and
- customwas evaporated to 5.5 Kg
- additionToluene:Isopropanol (2:3) was added
- customthe crystalline solid removed by filtration
- customdried
- customto give 12.6 Kg (61% over 2 steps), mp 124-126° C.