HRID1411379

反应详情

EQUATION

反应方程式

HRID 1411379 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
10 °C

PROCEDURE

实验过程

(R)-(+)-α,α-Diphenyl-2-pyrrolidinemethanol (1.08 g, 4.28 mmol) was dissolved in 70 mL of THF at ambient temperature in a dry flask under nitrogen and trimethyl borate (650 uL, 5.54 mmol) was added dropwise. The resulting solution was stirred for 1 hour. The solution was cooled in a cold bath to ˜10° C. and the N,N-diethylaniline borane (9.18 mL, 51.6 mmol) was added dropwise with some bubbling. After 15 minutes, this solution was transferred to an addition funnel and added dropwise to 1,4-bis(4-chloro-3-nitrophenyl)butane-1,4-dione (Intermediate 5B) (10.0 g, 25.2 mmol) suspended in 200 mL of THF and cooled to ˜10° C. Bubbling was observed. After the addition, the mixture was stirred at ambient temperature for 4 hours. The mixture was cooled in an ice bath and 30 mL or methanol was added dropwise until bubbling stopped, then the mixture was allowed to stir at ambient temperature for 30 minutes. The mixture was filtered to get rid of a trace of insoluble unreacted starting material. The filtrate was concentrated, poured into 1 N HCl and extracted into ethyl acetate, dried over sodium sulfate, and concentrated to give the title compound (9.9 g, 99%) as a yellow waxy solid. Chiral HPLC e.e. >99.9% (RR diol was undetectable). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.94 (d, J=1.9 Hz, 2H), 7.69 (d, J=8.4 Hz, 2H), 7.60 (dd, J=8.4, 1.9 Hz, 2H), 4.65 (m, 2H), 1.62 (m, 4H).

WORKUP

后处理

  1. waitAfter 15 minutes
  2. customthis solution was transferred to an addition funnel
  3. temperaturecooled to ˜10° C
  4. customBubbling
  5. additionAfter the addition
  6. stirringthe mixture was stirred at ambient temperature for 4 hours
  7. temperatureThe mixture was cooled in an ice bath
  8. addition30 mL or methanol was added dropwise
  9. customuntil bubbling
  10. stirringto stir at ambient temperature for 30 minutes
  11. filtrationThe mixture was filtered
  12. customto get
  13. concentrationThe filtrate was concentrated
  14. additionpoured into 1 N HCl
  15. extractionextracted into ethyl acetate
  16. dry with materialdried over sodium sulfate
  17. concentrationconcentrated