Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Anhydride → 3(-1-Acetoxytridecyl)-4-phenylfuran
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | 4-Phenyl-3-furaldehyde | HCID 15037148 | — |
| 반응물 | HCID 178443215 | HCID 178443215 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3(-1-Acetoxytridecyl)-4-phenylfuran | HCID 15037156 | — |
반응 단계
Dodecylmagnesium bromide (a 1.0M solution in THF; 2.11 ml, 2.11 mmol) was added to a solution of 4-phenyl-3-furaldehyde (303 mg, 1.76 mmol) in THF at 0 degrees under argon and gradually allowed to warm to room temperature with stirring. When all of the aldehyde was consumed acetic anhydride (719 mg, 7.04 mmol) was added and stirring was continued for 2 hours more. The reaction was quenched with saturated ammonium chloride and the organics were extracted into ethyl ether. The combined fractions were washed with saturated sodium bicarbonate, water and brine, dried over magnesium sulfate and concentrated to a yellow oil which was purified by flash chromatography on silica using 3% ethyl ether hexanes to give the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05268387 |
| 출처 데이터셋 | uspto-grants-1993_12 |
| ORD ID | ord-3eef5af2d972410ea16ff6997ef0445c |
| 출처 메모 | uspto-grants-1993_12 |