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HRID 1755968作成日:2026年10月27日

Hydrochloric Acid → 3-(Hexadecyloxy)-2-(tetradecyloxy)propan-1-OL

https://huagongshe.com/reaction/1755968

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Myristyl bromideHCID 8208—
反応物Potassium HydroxideHCID 14797—
反応物2,3-Bis(hexadecyloxy)propan-1-olHCID 102548—
反応物BenzylglycerolHCID 2735483—
反応物1-Hexadecyl-2-tetradecyl-3-trityl glycerolHCID 57129051—
溶媒TolueneHCID 1140—
生成物3-(Hexadecyloxy)-2-(tetradecyloxy)propan-1-OLHCID 57128111—

反応手順

1-hexadecyl glycerol (105 g, 0.33 mol) and 93 g (0.33 mol) tritylchloride were dissolved in 300 ml of pyridine. The mixture was heated at 100° C. for 16 hours. After cooling to room temperature 1500 ml of ethyl ether was added and the slurry washed 3 times with cold 0.5N H2SO4, 5% sodium bicarbonate and 2 times with water. The organic phase was dried over MgSO4, the ether removed on a rotary evaporator and the residue recrystallized from ethanol, yielding the intermediate 1-hexadecyl-3-trityl glycerol (129 g, 70%). The 2 position of this intermediate was alkylated with tetradecyl bromide in the same manner (powdered KOH in toluene) as described earlier for the dialkylation of benzyl glycerol in the preparation of 1,2-dihexadecyl glycerol. The resulting 1-hexadecyl-2-tetradecyl-3-trityl glycerol (128g) was dissolved in 300 ml of petroleum ether. At room temperature 30g of anhydrous hydrogen chloride was added. A precipitate formed within a short time. The slurry was stirred at room temperature for 4 hours and then filtered. The solids were recrystallized from acetone (10° C.) to give 45.6g of product, m.p. 42°-3° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05439669
出典データセットuspto-grants-1995_08
ORD IDord-da3bd6221bbd4f568006381924c4c0bf
出典メモuspto-grants-1995_08