化工社化工社 化学情報印刷レポート · 研究参考用
Diethyl Ether → rel-Methyl (1R,2S)-3-oxo-2-pentylcyclopentaneacetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Dimethyl Sulfate | HCID 6497 | — |
| 反応物 | (1S,2R)-3-oxo-2-pentyl-cyclopentaneacetic acid | HCID 16061083 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | rel-Methyl (1R,2S)-3-oxo-2-pentylcyclopentaneacetate | HCID 1738127 | 89.8% |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05728866 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-cb6326117e3045cb93e4c9a0471e9b58 |
| 出典メモ | uspto-grants-1998_03 |