참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Salicylamide | HCID 5147 | — |
| 반응물 | o-Toluenesulfonyl chloride | HCID 8623 | — |
| 반응물 | Sodium amide | HCID 24533 | — |
| 반응물 | 1-Methyl-3-pyrrolidinol | HCID 93074 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-[(1-Methyl-3-pyrrolidinyl)oxy]benzamide | HCID 13726283 | — |
반응 단계
To 85.6 g (2.2 moles) of sodium amide in 1.5 liter of dry toluene was added 202 g (2 moles) of 1-methyl-3-pyrrolidinol so as not to exceed a temperature of 50° C. The mixture was then heated to 70° C. for 4.5 hours. The mixture was cooled and 381 g (2 moles) of o-toluenesulfonylchloride was added at a rapid drop while maintaining a temperature of 20°-30° C. with an ice bath. The mixture was stirred at room temperature for 2.5 hours and washed with water. The toluene solution was dried with sodium sulfate and concentrated. The residue, dissolved in 500 ml of dimethylformamide, was added to a reaction mixture prepared by adding 119 g (2.2 moles) of sodium methoxide and 274 g (2.0 moles) of salicylamide to one liter of dimethylformamide and the mixture was worked up as in preparation 1. Yield of product was 170 g (38%), m.p. 116°-118° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04727152 |
|---|
| 출처 데이터셋 | uspto-grants-1988_02 |
|---|
| ORD ID | ord-b0c0fc9ef6e847a68cadcb68fa16fa36 |
|---|
| 출처 메모 | uspto-grants-1988_02 |
|---|