反应 #543536

ord-70b887f2c93f476bbdc39d8364937d2a

反应方程式

NC(=O)c1cc(Cl)ccc1O
5-chloro-2-hydroxybenzamide
c1ccncc1
pyridine
Cl
hydrochloric acid
CCOC(=O)Cl
Ethyl chloroformate
O=c1[nH]c(=O)c2cc(Cl)ccc2o1
6-chloro-2H-1,3-benzoxazine-2,4(3H)-dione
收率 85.3%

反应条件

温度
95°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.DISTILLATIONthe volatiles were distilled off (43 ml)
  2. 2
    温度The reaction was cooled to room temperature
  3. 3
    其他to form
  4. 4
    过滤The resulting solid was filtered
  5. 5
    其他recrystallized in hot ethanol

实验过程

A solution of 10 g of 5-chloro-2-hydroxybenzamide (58.0 mmol), pyridine (22 ml) and acetonitrile (25 ml) was stirred in an ice bath. Ethyl chloroformate (6.1 ml, 0.0638 mol) was added dropwise. The pink solution was stirred for 30 minutes at <10° C. The ice bath was replaced with an oil bath. The reaction mixture was heated to 95° C. and the volatiles were distilled off (43 ml). The reaction was cooled to room temperature, causing a white solid to form. The mixture was poured into water (100 ml) and acidified with concentrated aqueous hydrochloric acid. The resulting solid was filtered and recrystallized in hot ethanol to give 9.77 g of 6-chloro-2H-1,3-benzoxazine-2,4(3H)-dione.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07186414B2uspto-grants-2007_03