Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzyl Bromide → 4-Benzyloxyphenylacetonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzyl Bromide | HCID 7498 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-Hydroxybenzyl cyanide | HCID 26548 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-Benzyloxyphenylacetonitrile | HCID 522804 | 358.3% |
반응 단계
4-Hydroxybenzyl cyanide (2.5 g, 18.77 mmol), benzyl bromide (3.8 g, 22:5 mmol) and potassium carbonate (45 mmol) were combined in acetone (50 mL) and heated to reflux for 8 h. The reaction was allowed to cool to rt, diluted with ethyl acetate and filtered to remove the solids. The organic layer was concentrated in vacuo to give an oil. The crude benzyl ether was purified by chromatography on silica gel eluting hexane:ethyl acetate (90:10, v:v) to give 4-benzyloxybenzyl cyanide (4.0 g, 95%) which solidified. MS (M+NH4)+=241.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06610731B2 |
| 출처 데이터셋 | uspto-grants-2003_08 |
| ORD ID | ord-bc2d91ce438746bbbad4db8247c636a0 |
| 출처 메모 | uspto-grants-2003_08 |