HRID254688

反应详情

EQUATION

反应方程式

HRID 254688 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a vigorously stirred suspension of 1,17-diazido-3,6,9,12,15-pentaoxaheptadecane (25 g, 75 mmol) in 5% HCl (200 mL) was added a solution of triphenylphosphine (19.2 g, 73 mmol) in ether (150 mL) over 3 hrs at room temperature. The reaction mixture was stirred for additional 24 hrs. The phases were separated and the aqueous phase was extracted with dichloromethane (3×40 mL). The aqueous phase was cooled in an ice/water bath and the pH was adjusted to 12 by addition of solid potassium hydroxide. The aqueous phase was concentrated and the product was taken up in dichloromethane (150 mL). The organic phase was dried (Na2SO4) and concentrated giving of 22 g (95%) of a yellow oil. The product was identified by electrospray mass spectrometry (ESI-MS) (MH+ calculated: 307.19; found 307.4). The crude oil was used in the nest step without further purification.

WORKUP

后处理

  1. customThe phases were separated
  2. extractionthe aqueous phase was extracted with dichloromethane (3×40 mL)
  3. temperatureThe aqueous phase was cooled in an ice/water bath
  4. additionthe pH was adjusted to 12 by addition of solid potassium hydroxide
  5. concentrationThe aqueous phase was concentrated
  6. dry with materialThe organic phase was dried (Na2SO4)
  7. concentrationconcentrated