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Hexane → 12-(Methoxymethyl)oxy-3,7,11-trimethyl-2,6,10-dodecatrienal
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | 3,7,11-Trimethyl-12-(methoxymethyl)oxy-1,6,10-dodecatrien-3-ol | HCID 54127024 | — |
| 反応物 | HCID 178418287 | HCID 178418287 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 12-(Methoxymethyl)oxy-3,7,11-trimethyl-2,6,10-dodecatrienal | HCID 57206388 | 52% |
反応手順
A solution of 3,7,11-trimethyl-12-(methoxymethyl)oxy-1,6,10-dodecatrien-3-ol (460 mg, 1.6 mmol) in dichloromethane (30 ml) was added pyridinium chlorochromate (690 mg, 3.2 mmol), and the mixture was stirred at room temperature for 8 hours. After addition of a mixture of hexane, ethyl acetate, and ether (3:1:1) (100 ml), the mixture was stirred and insoluble materials were filtered. The filtrate was concentrated in vacuo, and the residue was purified with silica gel column chromatography to give 12-(methoxymethyl)oxy-3,7,11-trimethyl-2,6,10-dodecatrienal (233 mg, 52%). The physico-chemical properties of the product was the same as those described in Reference Example 1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05245085 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-be061f6076814d3eb2e7884b9794b2d8 |
| 出典メモ | uspto-grants-1993_09 |