反应 #952

ord-8c0bae38a8294d0e9674fa88542622fe

反应方程式

O=C(Cl)OCc1ccccc1
benzyl chloroformate
[N-]=[N+]=NCc1ccc(C(=N)N)cc1
( ii )
[N-]=[N+]=NCc1ccc(C(=N)N)cc1
4-amidino benzyl azide
CCN(CC)CC
triethyl amine
Cl
HCl
O=C(Cl)OCc1ccccc1
Benzyl chloroformate
[N-]=[N+]=NCc1ccc(C(=N)NC(=O)OCc2ccccc2)cc1
4-(benzyloxycarbonylamidino) benzyl azide

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    干燥the resulting solution was dried (K2CO3)
  2. 2
    过滤filtered
  3. 3
    温度was cooled in an ice bath
  4. 4
    干燥The organic phase was dried (MgSO4)
  5. 5
    其他the solvent was removed in vacuo

实验过程

The crystals from (ii) above were dissolved in 500 ml methylene chloride and the resulting solution was dried (K2CO3), filtered and 27 ml (194 mmol) triethyl amine was added. 25 ml Benzyl chloroformate was slowly added to the stirred solution while the reaction mixture was cooled in an ice bath. After 30 minutes an additional 2 ml benzyl chloroformate was added and stirring was continued for another 30 minutes. Subsequently, water was added and the aqueous phase was adjusted to pH 7 with 2M HCl. The organic phase was dried (MgSO4) and the solvent was removed in vacuo. 4-(benzyloxycarbonylamidino) benzyl azide was finally isolated as colorless crystals from ether/methylene chloride/hexane.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723444uspto-grants-1998_03