Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Acid → Dimethyl [3-(3-chlorophenyl)-2-oxopropyl]phosphonate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Dimethyl methylphosphonate | HCID 12958 | — |
| 반응물 | Methyl 2-(3-chlorophenyl)acetate | HCID 2733544 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Dimethyl [3-(3-chlorophenyl)-2-oxopropyl]phosphonate | HCID 12989750 | 23.3% |
반응 단계
To a solution of dimethyl methylphosphonate (17.93 g, 144 mmol) in THF (270 mL) at −78° C. was slowly added n-BuLi (2.5M, 64.2 mL, 160.6 mmol). The reaction mixture was stirred for 1 h and (3-chloro-phenyl)-acetic acid methyl ester (26.93 g, 146 mmol) was slowly added. The reaction mixture was allowed to warm to room temperature and was stirred for 24 h. Acetic acid (15 mL) was added and the volatiles were removed in vacuo. The residue was diluted with CH2Cl2 and the organic solution was washed carefully with saturated aqueous NaHCO3 (3 times). The organic layer was dried (MgSO4), filtered and concentrated in vacuo. Purification by medium pressure chromatography (20% EtOAc in hexanes to EtOAc) provided the title compound (9.28 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07192979B2 |
| 출처 데이터셋 | uspto-grants-2007_03 |
| ORD ID | ord-2a19f2ecff17431880410c53b34f053b |
| 출처 메모 | uspto-grants-2007_03 |