戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1377118作成日:2026年10月26日

Methanol → 3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraen-1-ol

https://huagongshe.com/reaction/1377118

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物WaterHCID 962—
反応物Potassium HydroxideHCID 14797—
反応物Geranylgeranyl octadecanoateHCID 14413715—
溶媒HexaneHCID 8058—
生成物3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraen-1-olHCID 86591503100%

反応条件

温度50 °C

反応手順

250 g of methanol, 4.7 g of potassium hydroxide and 10 g of water were added to 23.0 g of geranylgeranyl stearate (containing 22.08 g of geranylgeranyl stearate and 0.37 g of geranylneryl stearate) obtained as a cake in Example 2. The reaction mixture was stirred at 50° C. for 1 hour and cooled down to room temperature, to which 130 g of hexane was added. The resulting organic phase was separated, and the aqueous phase (lower phase) was washed twice with 120 g of hexane. Thereafter, the hexane washings were combined to the organic phase, followed by washing twice with 100 g of a 50% aqueous methanol. The resultant organic phase was concentrated under reduced pressure to give 12 g of crude geranylgeraniol. This crude product was subjected to simple distillation (137° C., 0.3 mmHg) to give 8.2 g of a main fraction. The results of the analysis of the obtained fraction with gas chromatography revealed that it contained geranylgeraniol with a purity of 98.1% and geranylnerol with a purity of 1.2%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05663461
出典データセットuspto-grants-1997_09
ORD IDord-19ae2a9dbe1b4bba8351e3b12ac155b6
出典メモuspto-grants-1997_09