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HRID 231256作成日:2026年10月26日

6-Mercapto-1-hexanol → 2-Methoxy-3-octadecyloxypropyl 6-hydroxyhexyl sulfide

https://huagongshe.com/reaction/231256

反応式

関与物質

役割名称HCID仕込み量
反応物6-Mercapto-1-hexanolHCID 560126—
反応物Sodium borohydrideHCID 4311764—
反応物Sodium MethoxideHCID 10942334—
反応物2-Methoxy-3-octadecyloxypropyl methanesulfonateHCID 14501037—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2-Methoxy-3-octadecyloxypropyl 6-hydroxyhexyl sulfideHCID 1450103897.5%

反応手順

To 14 ml of a methanol solution of sodium methoxide (1M solution) are added 2.04 g of 6-mercaptohexanol and 0.24 g of sodium borohydride, to which a THF (20 ml) solution containing 2.18 g of 2-methoxy-3-octadecyloxypropyl methanesulfonate is added dropwise under nitrogen streams with stirring. The mixture is stirred at room temperature for 20 hours and then at 40° C. for 1 hour. After the addition of water, the mixture is extracted with ethyl acetate. The extracted layer is washed with water, dried and concentrated under reduced pressures to obtain an oily product. Purification of the oily product by silica gel column chromatography gives 2.31 g of the captioned compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04845219
出典データセットuspto-grants-1989_07
ORD IDord-4c91898a85ad49d3857d98c9dbfe87a3
出典メモuspto-grants-1989_07