Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Bromoquinoline → 3-(Dimethoxyacetyl)quinoline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Bromoquinoline | HCID 21413 | — |
| 반응물 | N-(dimethoxyacetyl)morpholine | HCID 21298597 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(Dimethoxyacetyl)quinoline | HCID 14276934 | — |
반응 단계
3-Bromoquinoline (3.29 ml., 0.032 mol) was dissolved in 300 ml. THF and cooled to -78°. n-Butyllithium (13.6 ml. of 2.5M in hexane, 0.034 ml.) was added slowly and the mixture stirred 15 minutes at -75° to -78°. N-(Dimethoxyacetyl)morpholine (5.98 g., 0.032 mol) in 10 ml. THF was then added and stirring continued for 1.75 hours at the same temperature. The reaction was then quenched into 300 ml. saturated NH4Cl. The aqueous layer was separated and extracted 4×100 ml. ether. The organic layers were combined, dried over MgSO4, stripped to yield title product, 7.0 g., bp 120°-123°/0.125 torr.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04762921 |
| 출처 데이터셋 | uspto-grants-1988_08 |
| ORD ID | ord-97c01dee82af4b81ba08bf372d90172a |
| 출처 메모 | uspto-grants-1988_08 |