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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1755968생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1755968

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Myristyl bromideHCID 8208—
반응물Potassium HydroxideHCID 14797—
반응물2,3-Bis(hexadecyloxy)propan-1-olHCID 102548—
반응물BenzylglycerolHCID 2735483—
반응물1-Hexadecyl-2-tetradecyl-3-trityl glycerolHCID 57129051—
용매TolueneHCID 1140—
생성물3-(Hexadecyloxy)-2-(tetradecyloxy)propan-1-OLHCID 57128111—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05439669
출처 데이터셋uspto-grants-1995_08
ORD IDord-da3bd6221bbd4f568006381924c4c0bf
출처 메모uspto-grants-1995_08