반응 #323322
ord-94bd98665d3840b983c849869e2fcac7
반응 방정식
용매
반응 조건
후처리
- 1온도to reflux for 18 hr
- 2여과the solution filtered
- 3농축concentrated
- 4여과filtered
- 5농축The filtrate was concentrated
- 6기타the residue (which crystallized)
- 7온도was refluxed with 300 ml of thionyl chloride for 0.5 hr
- 8농축and concentrated in vacuo
- 9workup.DISSOLUTIONThe residue was dissolved in 300 ml of chloroform
- 10workup.DISSOLUTIONThe residue was redissolved in chloroform
- 11workup.ADDITION150 ml of triethyl amine added
- 12온도the mixture refluxed 1 hr
- 13농축The solution was concentrated in vacuo
- 14기타the residue partitioned between 400 ml of ethyl acetate, 400 ml of isopropyl ether and 500 ml of dilute hydrochloric acid
- 15세척The organic layer was washed twice with water and once with dilute sodium hydroxide
- 16건조dried with sodium sulfate
- 17농축concentrated
- 18기타The residue was crystallized from isopropanol-water
실험 절차
To 54 g (1.35 mole) of sodium hydroxide in 800 ml of water was added 148 g (0.67 mole) of 2-[(1-methyl-3-pyrrolidinyl)oxy]benzamide and the mixture brought to reflux for 18 hr. The pH was adjusted to 7 with hydrochloric acid and the solution filtered and concentrated. The residue was boiled with 400 ml of isopropanol and filtered. The filtrate was concentrated and the residue (which crystallized) was refluxed with 300 ml of thionyl chloride for 0.5 hr. and concentrated in vacuo. The residue was dissolved in 300 ml of chloroform and the solvent boiled off in vacuo. The residue was redissolved in chloroform, 150 ml of triethyl amine added and the mixture refluxed 1 hr. The solution was concentrated in vacuo and the residue partitioned between 400 ml of ethyl acetate, 400 ml of isopropyl ether and 500 ml of dilute hydrochloric acid. The organic layer was washed twice with water and once with dilute sodium hydroxide, dried with sodium sulfate and concentrated. The residue was crystallized from isopropanol-water. Yield of product was 75 g (47%), m.p. 97°-107° C.