反応 #4895

反応方程式

2-[(1-benzyl-3-pyrrolidinyl)oxy]-benzoic acid

thionyl chloride

triethylamine

→

4-Benzyl-2-(2-chloroethyl)-2,3-dihydro-1,4-benzoxazepin-5(4H)-one

反応条件

後処理

1. 1
   温度was then refluxed 30 min.
2. 2
   濃縮concentrated in vacuo
3. 3
   workup.ADDITIONThe residue was twice treated with 250 ml of chloroform
4. 4
   濃縮concentrated in vacuo
5. 5
   workup.DISSOLUTIONThe residue was dissolved in 500 ml of chloroform
6. 6
   温度The solution was refluxed 1 hr
7. 7
   濃縮and concentrated in vacuo
8. 8
   その他The residue was partitioned between 50% ethyl acetate-50% isopropyl ether and dilute hydrochloric acid
9. 9
   洗浄The organic layer was washed with dilute sodium hydroxide
10. 10
    濃縮concentrated
11. 11
    その他The residue was crystallized 5 times from isopropyl ether-ethyl acetate

実験手順

To 85.7 g (0.29 mole) of 2-[(1-benzyl-3-pyrrolidinyl)oxy]-benzoic acid was added 150 ml of thionyl chloride. The solution stood for 15 min and was then refluxed 30 min. and concentrated in vacuo. The residue was twice treated with 250 ml of chloroform and concentrated in vacuo. The residue was dissolved in 500 ml of chloroform and 101 g (1 mole) of triethylamine added slowly with stirring. The solution was refluxed 1 hr. and concentrated in vacuo. The residue was partitioned between 50% ethyl acetate-50% isopropyl ether and dilute hydrochloric acid. The organic layer was washed with dilute sodium hydroxide and concentrated. The residue was crystallized 5 times from isopropyl ether-ethyl acetate. Yield of product was 23.8 g (26%), m.p. 145.0°-147° C.

出典