Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Epichlorohydrin → 2-[(4-Benzoylphenoxy)methyl]oxirane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Epichlorohydrin | HCID 7835 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-Hydroxybenzophenone | HCID 14347 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 2-[(4-Benzoylphenoxy)methyl]oxirane | HCID 352816 | — |
반응 단계
As illustrated in FIG. 6, 100 mL of dried acetone were added to a dry, 250-mL round bottom flask, equipped with a magnetic stirrer, along with 15.05 grams of 4-hydroxybenzophenone, 32.1 grams of epichlorohydrin, and 6.2 grams of potassium carbonate. The solution was heated to reflux for 6 hours and then cooled to room temperature. The precipitated potassium chloride was filtered off, and the solution was evaporated to remove excess epichlorohydrin. The crude product was recrystallized from methanol. 1H NMR data confirmed the formation of the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07045366B2 |
| 출처 데이터셋 | uspto-grants-2006_05 |
| ORD ID | ord-11abb5634ed142ee9bd12b16b8fc0da6 |
| 출처 메모 | uspto-grants-2006_05 |