반응 #42190

반응 방정식

imidazole

(±)-3-[4-(benzyloxy)-2,3-dihydro-1H-inden-5-yl]propane-1,2-diol

tert-butyldimethylsilyl chloride

→

(±)-1-[4-(benzyloxy)-2,3-dihydro-1H-inden-5-yl]-3-{[tert-butyl(dimethyl)silyl]oxy}propan-2-ol

수율 73.1%

용매

N,N-dimethylformamide

반응 조건

후처리

1. 1
   기타The reaction mixture was quenched with methanol (5 mL)
2. 2
   workup.ADDITIONdiluted with diethyl ether (500 mL)
3. 3
   세척The organic layer was washed with aqueous hydrogen chloride (200 mL, 0.5 N), water (3×200 mL), saturated aqueous sodium chloride (200 mL)
4. 4
   건조dried (magnesium sulfate)
5. 5
   기타the solvent was removed in vacuo
6. 6
   기타to provide a crude oil
7. 7
   기타Purification by flash column chromatography (silica, ethyl acetate:hexanes 1:4)

실험 절차

To a solution of (±)-3-[4-(benzyloxy)-2,3-dihydro-1H-inden-5-yl]propane-1,2-diol (9.10 g, 30.5 mmol) in N,N-dimethylformamide (150 mL) was added tert-butyldimethylsilyl chloride (4.83 g, 32.04 mmol) followed by imidazole (2.49 g, 36.60 mmol) and the reaction mixture was allowed to stir at room temperature overnight. The reaction mixture was quenched with methanol (5 mL) and diluted with diethyl ether (500 mL). The organic layer was washed with aqueous hydrogen chloride (200 mL, 0.5 N), water (3×200 mL), saturated aqueous sodium chloride (200 mL), dried (magnesium sulfate) and the solvent was removed in vacuo to provide a crude oil. Purification by flash column chromatography (silica, ethyl acetate:hexanes 1:4) gave 9.20 g (73%) of (±)-1-[4-(benzyloxy)-2,3-dihydro-1H-inden-5-yl]-3-{[tert-butyl(dimethyl)silyl]oxy}propan-2-ol as a colorless oil. Rf=0.37 (silica, ethyl acetate:hexanes 1:4); Anal. calcd. for C25H36O3Si: C, 72.77; H, 8.79. Found: C, 72.3; H, 8.48.

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