Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Aluminium lithium hydride → [2-(4-Bromo-phenyl)4-isopropyl-oxazol-5-yl]-methanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 반응물 | 2-(4-Bromo-phenyl)4-isopropyl-oxazole-5-carboxylic acid ethyl ester | HCID 69053256 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [2-(4-Bromo-phenyl)4-isopropyl-oxazol-5-yl]-methanol | HCID 69056838 | 99.2% |
반응 단계
A solution of 2-(4-bromo-phenyl)-4-isopropyl-oxazole-5-carboxylic acid ethyl ester (20.6 g, 60.9 mmol) in THF (300 mL) is cooled in an ice-water bath and treated portionwise with LiAlH4 (2.8 g, 73 mmol). The reaction is complete after 1.5 h. Ice chips (˜10 g) are added to quench the excess hydride reagent, and anhydrous Na2SO4 (˜50 g) is added. The thick suspension is stirred 30 min, filtered through celite, and washed with ThF (600 mL). The filtrate is dried (Na2SO4) and concentrated. The crude product is purified by silica gel flash chromatography using hexanes:ethyl acetate (3:1) to give a white solid (17.9 g, 99%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07528160B2 |
| 출처 데이터셋 | uspto-grants-2009_05 |
| ORD ID | ord-00916f7c763b4ad4a606108189afe6e2 |
| 출처 메모 | uspto-grants-2009_05 |