反应 #2267062

ord-637a8e46faa74e069f5f6b0a971fe3e1

反应方程式

ICCc1ccccc1
Phenethyl iodide
COCCOC
DME
II
I2
OC1(CCc2ccccc2)CCCCC1
phenethylcyclohexanol
收率 96.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他at room temperature

实验过程

Since TmI2(DME)x exhibits such high reactivity at room temperature, its viability at reduced temperature is examined. In these reactions, TmI2(DME)x is added as a DME solution by syringe using a saturated stock solution generated in situ from Tm and I2. Phenethyl iodide reacts smoothly at −22° C. in 10 minutes to form phenethylcyclohexanol in 96% yield (entry f). The reaction of phenethyl bromide with cyclohexanone at 0° C. produces a 96% yield of phenethylcyclohexanol in 20 minutes (entry g), while reaction at −22° C. gave a 94% yield in 60 minutes (entry h). Phenethyl chloride reacts at 0° C. to give a 90% yield after 1 hour (entry j). This variation of reaction time as a function of temperature could be used to control regiochemistry in sequenced reactions.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06887824B1uspto-grants-2005_05