Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Boron trifluoride → 3-Cyclopentyl-2-methoxy-3-oxo-propionic acid methyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Boron trifluoride | HCID 6356 | — |
| 반응물 | Ethyl 3-cyclopentyl-3-oxopropanoate | HCID 11159709 | — |
| 반응물 | Acetic acid;iodosylbenzene | HCID 73357407 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 3-Cyclopentyl-2-methoxy-3-oxo-propionic acid methyl ester | HCID 59777286 | — |
반응 단계
The title compound was prepared using a method analogous to that described in Tetrahedron 1998, 44, 1603-1607: To a suspension of iodosobenzene diacetate (5.2 g, 16.3 mmol) in MeOH (40 mL) was added BF3.0Et2 (2.1 mL, 16.3 mmol). The resulting mixture was added to 3-cyclopentyl-3-oxo-propionic acid ethyl ester (3.0 g, 16.3 mmol) and stirred at rt overnight. The mixture was concentrated to half the total volume, quenched with satd. aq. NaHCO3, and extracted with CHCl3 (2×). The combined organic layers were dried and concentrated and the crude residue purified (EtOAc/hexanes) to yield a colorless oil (1.5 g, 43%). 1H NMR (MeOD): 4.4 (s, 1H), 3.8 (s, 3H), 3.5 (s, 3H), 3.3-3.2 (m, 1H), 1.9-1.5 (m, 8H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08686142B2 |
| 출처 데이터셋 | uspto-grants-2014_04 |
| ORD ID | ord-67374e29976643d285c7ad4bdfe39613 |
| 출처 메모 | uspto-grants-2014_04 |