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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2290808생성일: 2026년 10월 26일

Hydrochloric Acid → 11-Benzyloxy-1-(3,4-dibenzyloxyphenyl)-1-undecanol

https://huagongshe.com/reaction/2290808

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodineHCID 807—
반응물IodoethaneHCID 6340—
반응물3,4-Bis(benzyloxy)benzaldehydeHCID 79526—
반응물MagnesiumHCID 5462224—
반응물10-Benzyloxy-1-chlorodecaneHCID 11065932—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물11-Benzyloxy-1-(3,4-dibenzyloxyphenyl)-1-undecanolHCID 1355788546.8%

반응 단계

To a mixture of 1 ml of anhydrous ether and 0.6 g of metallic magnesium were added 0.1 ml of ethyl iodide and a piece of iodine crystal followed by heating to initiate the reaction and then a mixture of 6.7 g of 10-benzyloxy-1-chlorodecane and 10 ml of anhydrous ether was added dropwise to the aforesaid mixture. After the reaction was over, the reaction mixture was refluxed for 2 hours. After cooling, the reaction mixture was added dropwise to a solution of 6 g of 3,4-dibenzyloxybenzaldehyde dissolved in 30 ml of tetrahydrofuran at 0° to 5° C. Thereafter, the mixture was stirred for 30 minutes at room temperature and after adding 300 ml of an aqueous 1% hydrochloric acid solution to the reaction mixture, the product was extracted with 100 ml of toluene. The extract was washed with water, dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was dissolved in 30 ml of ethanol, the solution was allowed to stand overnight under cooling to 0° to 5° C., and the crystals thus precipitated were collected by filtration. By drying the crystals, 5 g of 11-benzyloxy-1-(3,4-dibenzyloxyphenyl)-1-undecanol was obtained. Melting point 50°-52° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04618627
출처 데이터셋uspto-grants-1986_10
ORD IDord-f8ef0e71b7b946dbb6e2984cbafbd147
출처 메모uspto-grants-1986_10