化工社化工社 化学情報印刷レポート · 研究参考用
HRID 132099作成日:2026年10月26日
3-Oxo-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester → 3-Methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester
https://huagongshe.com/reaction/132099
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-Oxo-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester | HCID 59733780 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 触媒 | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Acetate | HCID 175 | — |
| 生成物 | 3-Methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester | HCID 59733752 | 100% |
反応手順
A solution of 1.6 M n-butyllithium in hexanes (14.0 mL, 22.4 mmol) was added to a heterogeneous mixture of methyltriphenylphosphonium bromide (8.02 g, 22.4 mmol) in tetrahydrofuran (50 mL) at −10° C. After stirring for 30 min at −10° C., the yellow slurry was cooled to −78° C. and 3-oxo-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester (3.41 mg, 14.1 mmol) in tetrahydrofuran (20 mL) was added. After stirring for 10 min at −78° C., the dry ice/acetone bath was removed and the heterogeneous mixture was stirred for 3 h, during which time the solution warmed to ambient temperature. The heterogeneous mixture was concentrated and the residue was flash chromatographed with 99:1, 49:1, 24:1, and 23:2 hexanes:etheyl acetate as the eluant to yield 3.38 g (100% yield) of 3-methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester as a clear oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07385085B2 |
|---|
| 出典データセット | uspto-grants-2008_06 |
|---|
| ORD ID | ord-2574301570b546bbbd04d4f66b8d5256 |
|---|
| 出典メモ | uspto-grants-2008_06 |
|---|