反应 #1540

ord-2b0378d7412b4bedb3ed0ed2242b2a38

反应方程式

Cl.N=C(N)c1ccccc1.O
benzamidine hydrochloride hydrate
CC(=O)[O-].[Na+]
sodium acetate
CCOC(=O)C=C(OCC)OCC
ethyl 3,3-diethoxyacrylate
CS(C)=O
DMSO
CCOc1cc(=O)[nH]c(-c2ccccc2)n1
6-ethoxy-2-phenyl-4(3H)-pyrimidinone
收率 57.0%

溶剂

反应条件

温度
120°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The mixture was cooled
  2. 2
    洗涤washed with two 100 mL portions of ether
  3. 3
    过滤the precipitate was collected by filtration
  4. 4
    其他dried under vacuum at 50° C.

实验过程

A mixture of 3.14 g (20.0 mmol) of benzamidine hydrochloride hydrate, 1.65 g (20.1 mmol) of powdered anhydrous sodium acetate, 4.17 g (22.2 mmol) of ethyl 3,3-diethoxyacrylate and 10 mL of DMSO was heated at 120° C. for 8 h. The mixture was cooled, diluted with 50 mL of 5% aqueous NaOH and washed with two 100 mL portions of ether. The aqueous layer was acidified with concentrated hydrochloric acid and the precipitate was collected by filtration and dried under vacuum at 50° C. to furnish 2.28 g (57%) of crude 6-ethoxy-2-phenyl-4(3H)-pyrimidinone as a yellow solid 1 H-NMR (d6-DMSO) δ 1.35(3H,t), 4.33(2H,q), 5.60(1H,s), 7.50(3H,m), 8.2(2H,m).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05726124uspto-grants-1998_03