Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diethyl Ether → rel-Methyl (1R,2S)-3-oxo-2-pentylcyclopentaneacetate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Dimethyl Sulfate | HCID 6497 | — |
| 반응물 | (1S,2R)-3-oxo-2-pentyl-cyclopentaneacetic acid | HCID 16061083 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | rel-Methyl (1R,2S)-3-oxo-2-pentylcyclopentaneacetate | HCID 1738127 | 89.8% |
반응 단계
To 104 mg (0.49 mmole) of (±)cis-3-oxo-2-pentyl-1-cyclopentaneacetic acid (93:7 cis/trans ratio) in 1 ml of (CH3)2CO there were added, first 56 μl of (CH3)2SO4 (74 ml, 0.59 mmole, 1.2 eq.) and then 81 mg (0.59 mmole, 1.2 eq.) of anhydrous solid K2 CO3. The resulting suspension was heated at r.t. during 4 h and taken in water and with ether. The ether phase was separated and the aqueous phase once more extracted with ether. The combined organic phases were washed with water, dried over MgSO4, filtered and concentrated. The residue was distilled in a bulb-to-bulb apparatus (oven t.: 180°/7 Pa) to provide 93 mg (0.44 mmole, yield 84%) of methyl (±)-cis-3-oxo-2-pentyl-1-cyclopentaneacetate (92/8 cis/trans ratio).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05728866 |
| 출처 데이터셋 | uspto-grants-1998_03 |
| ORD ID | ord-cb6326117e3045cb93e4c9a0471e9b58 |
| 출처 메모 | uspto-grants-1998_03 |