Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium Hydroxide → 2-{3-[2-(2-Methoxyethoxy)ethoxy]phenyl}oxirane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Trimethylsulfonium methyl sulfate | HCID 2760871 | — |
| 반응물 | 3-[2-(2-Methoxyethoxy)ethoxy]benzaldehyde | HCID 22574324 | — |
| 촉매 | Tetrabutylammonium Bromide | HCID 74236 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Sodium chloride; water | HCID 57417360 | — |
| 생성물 | 2-{3-[2-(2-Methoxyethoxy)ethoxy]phenyl}oxirane | HCID 22574382 | 126.9% |
반응 단계
To a stirred solution of 1.32 g of 3-[2-(2-methoxyethoxy)ethoxy]benzaldehyde and 15 mg of tetra-n-butylammonium bromide in 15 ml of CH2Cl2 is added a solution of 2.4 g of trimethylsulfonium methylsulfate in 4 ml of water, followed by 10 ml of 50% NaOH. The mixture is stirred and refluxed for 4 h, then cooled, diluted with ether and brine, and filtered. The organic phase is washed with brine, dried (MgSO4), and concentrated under reduced pressure to provide 1.78 g of the title compound as a pale yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06852731B2 |
| 출처 데이터셋 | uspto-grants-2005_02 |
| ORD ID | ord-212bfc66156440dcb496d984dc7e2eed |
| 출처 메모 | uspto-grants-2005_02 |