Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Cinnamic Acid → 4-tert-butyl-10,10-dimethyl-3,6-dioxo-2,7-dioxa-4-aza-10-silaundec-1-yl (2E)-3-phenylacrylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Cinnamic Acid | HCID 444539 | — |
| 반응물 | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| 반응물 | 2-(Trimethylsilyl)ethyl 2-(tert-butyl((chloromethoxy)carbonyl)amino)-acetate | HCID 86611019 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 4-tert-butyl-10,10-dimethyl-3,6-dioxo-2,7-dioxa-4-aza-10-silaundec-1-yl (2E)-3-phenylacrylate | HCID 58826179 | — |
반응 단계
Trans-cinnamic acid (23.1 mmol) and 1.0 M tetrabutylammonium hydroxide (22.2 mmol) in methanol are stirred for one hour, and the methanol is removed. THF is added. To this solution is added 2-(trimethylsilyl)ethyl 2-(tert-butyl((chloromethoxy)carbonyl)amino)-acetate (18.5 mmol) and the mixture is stirred at room temperature for 24 hr. The solvent is removed and the residue is diluted with ether. The resulting solution is washed with water and brine. The organic layer is dried over magnesium sulfate, filtered and concentrated under reduced pressure to yield 5.01 g (61%) MS (ESI) m/z 436.3.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08101590B2 |
| 출처 데이터셋 | uspto-grants-2012_01 |
| ORD ID | ord-43c9a01e833442d19214623c988353dc |
| 출처 메모 | uspto-grants-2012_01 |