반응 #47278

반응 방정식

water

((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methanol

1,4-diazabicyclo[2.2.2]octane

4-chlorobenzenesulfonyl chloride

→

4-chloro-benzenesulfonic acid (S)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester

수율 93.3%

용매

ethyl acetate

heptane

heptane

반응 조건

후처리

1. 1
   workup.ADDITIONwas added
2. 2
   workup.STIRRINGthe resulting mixture stirred at room temperature overnight
3. 3
   기타the organic layer was separated
4. 4
   세척washed with water (3×600 mL)
5. 5
   농축The mixture was concentrated under vacuum
6. 6
   기타to provide a yellow oil which
7. 7
   농축The mixture was concentrated
8. 8
   기타to remove any remaining ethyl acetate and heptane (500 mL)
9. 9
   workup.ADDITIONwas added once more
10. 10
    기타crystallization
11. 11
    여과The thick white suspension was filtered
12. 12
    세척washed with heptane, and suction
13. 13
    기타dried

실험 절차

To a solution of ((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methanol (60.00 g, 454.0 mmol) and 1,4-diazabicyclo[2.2.2]octane (63.67 g, 567.6 mmol) in ethyl acetate 600 mL) at 15° C. was added 4-chlorobenzenesulfonyl chloride (100.6 g, 476.7 mmol) and the resulting cloudy solution stirred for 2 h before being warmed to room temperature. The resulting solution was stirred at room temperature for 4 h before cold water (300 mL) was added and the resulting mixture stirred at room temperature overnight. The mixture was diluted with heptane (600 mL) and the organic layer was separated and washed with water (3×600 mL). The mixture was concentrated under vacuum to provide a yellow oil which was treated with heptane (200 mL). The mixture was concentrated to remove any remaining ethyl acetate and heptane (500 mL) was added once more to induce crystallization. The thick white suspension was filtered, washed with heptane, and suction dried to provide 4-chloro-benzenesulfonic acid (S)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester (129.93 g, 93.3%, 98.9% pure HPLC, 99.89% e.e) as a white solid.

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