関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | (2-Carboxyethyl)triphenylphosphonium chloride | HCID 10270534 | — |
| 反応物 | 9,10-Dihydro-9,10-methanoanthracene-9-carboxaldehyde | HCID 12404141 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | gamma-(9,10-Dihydro-9,10-methano-9-anthryl)-beta-butenoic acid | HCID 54474651 | — |
反応手順
To a mixture of 9-formyl-9,10-dihydro-9,10-methanoanthracene (110 mg) and β-carboxyethyltriphenylphosphonium chloride (186 mg) in dimethylsulfoxide (2 ml) and tetrahydrofuran (2 ml) was added 65.4% sodium hydride dispersion in mineral oil (37 mg) at 0° C. under nitrogen. The reaction mixture was stirred at 0° C. for 6 hours, diluted with water, acidified with hydrochloric acid and extracted with benzene. The benzene extract was shaken with 2 N aqueous sodium hydroxide. The basic layer was acidified with hydrochloric acid and extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried over anhydrous sodium sulfate and evaporated to dryness to give γ-(9,10-dihydro-9,10-methano-9-anthryl)-β-butenoic acid. M.P. 166°-167° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04224344 |
|---|
| 出典データセット | uspto-grants-1980_09 |
|---|
| ORD ID | ord-6a1bcab99e7646dca3cfbb7012c89a4b |
|---|
| 出典メモ | uspto-grants-1980_09 |
|---|