Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
18-Crown-6 → 1-(2-Methoxyethenyl)-4-(octyloxy)benzene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 18-Crown-6 | HCID 28557 | — |
| 반응물 | p-(Octyloxy)benzaldehyde | HCID 90358 | — |
| 반응물 | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 1-(2-Methoxyethenyl)-4-(octyloxy)benzene | HCID 53775512 | — |
반응 단계
Potassium t-butoxide (1.9 g) is added to a slurry of methoxymethyl triphenylphosphonium chloride (6.17 g) and 18-Crown-6 (100 mg) in dry THF (40 ml). The mixture is stirred for 5 min, cooled to 15°, and a solution of 4-octyloxybenzaldehyde (3.52 g) in THF (5 ml) is added dropwise. The reaction mixture is stirred at room temperature for 20 min, diluted with 250 ml hexane, and the resulting mixture filtered through a pad of diatomaceous earth. Evaporation of the filtrate leaves crude 1-(2-methoxyethenyl)-4-(octyloxy)benzene as a mixture of cis and trans isomers, containing about 15 mol % triphenylphosphine oxide. The crude material may be used as is, or may be chromatographed with 1:1 hexanedichloromethane.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05464865 |
| 출처 데이터셋 | uspto-grants-1995_11 |
| ORD ID | ord-342bcfb170dd446095d890ba2b2078d3 |
| 출처 메모 | uspto-grants-1995_11 |