化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → rac-(1R*,4R*)-6-methyl-5-propyl-bicyclo[2.2.2]oct-5-en-2-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Hexanone | HCID 11583 | — |
| 反応物 | 2-Cyclohexen-1-one | HCID 13594 | — |
| 反応物 | Phosphorus oxide (P4O10) | HCID 14812 | — |
| 反応物 | Trifluoromethanesulfonic acid | HCID 62406 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | rac-(1R*,4R*)-6-methyl-5-propyl-bicyclo[2.2.2]oct-5-en-2-one | HCID 68414355 | — |
反応手順
Prepared using the method described in Jung, Michael E.; Tetrahedron Letters 2005, 46(30), 5057-5061. To a suspension of 2.8 g of phosphorous pentoxide in 30 mL anh. DCM were added 6.1 mL of 2-hexanone followed by 14.4 mL of 2-cyclohexen-1-one at rt. The suspension was cooled to 0° C. with an ice bath before 13 mL of trifluoromethanesulfonic acid was carefully added. The reaction mixture was warmed to rt and then heated at 40° C. overnight. 27 mL of NEt3 were dropwise added at 0° C., the mixture was stirred at rt for 10 min and then evaporated to dryness. Purification by CC with EtOAc-Hept (25:75) yielded 3.37 g of rac-(1R*,4R*)-6-methyl-5-propyl-bicyclo[2.2.2]oct-5-en-2-one as brown oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08202885B2 |
| 出典データセット | uspto-grants-2012_06 |
| ORD ID | ord-f6ef2aac6ebd4c6c9b699b0cedcabd62 |
| 出典メモ | uspto-grants-2012_06 |