Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Citric Acid → 2-Bromo-1-[3-tert-butyl-5-(2-methoxyethoxy)phenyl]ethanone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Citric Acid | HCID 311 | — |
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| 반응물 | 1-[3-Tert-butyl-5-(2-methoxyethoxy)phenyl]ethanone | HCID 58136808 | — |
| 용매 | MeOH tetrahydrofuran | HCID 21899815 | — |
| 생성물 | 2-Bromo-1-[3-tert-butyl-5-(2-methoxyethoxy)phenyl]ethanone | HCID 58136782 | 292.5% |
반응 단계
1-[3-tert-Butyl-5-(2-methoxyethoxy)phenyl]ethanone (O2.043; 1 g) was dissolved in methanol/THF (25 ml/25 ml), admixed with phenyltrimethylammonium tribromide (882 mg) while stirring and stirred at RT overnight. Then 50 ml of 20% citric acid solution were added and the mixture was stirred for 1 h. Subsequently, DCM (200 ml) was added and the mixture was extracted three times with DCM. Then the combined DCM phases were dried over magnesium sulfate, filtered and concentrated. The residue was purified using silica gel (40 g cartridge, n-heptane/EA gradient of 0-30% in 30 min). 1.31 g of the title compound were obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08198272B2 |
| 출처 데이터셋 | uspto-grants-2012_06 |
| ORD ID | ord-a25aebc613cf4db3876963c6003ed612 |
| 출처 메모 | uspto-grants-2012_06 |