반응 #2027414

ord-978a4208eea748f68b2d38d2ea23ffa7

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타A three-neck 500-mL flask equipped with a thermometer, a mechanical stirrer, an addition funnel, a condenser
  2. 2
    workup.ADDITIONDuring the addition period
  3. 3
    기타the flask was immersed in an ice bath
  4. 4
    온도to maintain the reaction temperature at 21.5° C. to 25.5° C. for 2.1 hours
  5. 5
    기타The acid layer was removed
  6. 6
    세척washed once with 30 mL EDC
  7. 7
    기타The combined EDC solutions were quenched with 2% NaHCO3 (600 mL)
  8. 8
    세척washed with deionized water (400 mL), 1% NaHCO3 solution (400 mL), deionized water (400 mL

실험 절차

A three-neck 500-mL flask equipped with a thermometer, a mechanical stirrer, an addition funnel, a condenser, and a positive nitrogen atmosphere was charged with 1,4-dichloro-2,3-butanediol (50.0 g, 0.314 mole), trioxane (9.43 g, 0.314 mole), and 1,2-dichloroethane (EDC) (300 mL). The 1,4-dichloro-2,3-butanediol was not totally dissolved. Concentrated sulfuric acid (46.3 g, 0.455 mole) was then added dropwise over eight minutes. During the addition period, a slight exotherm was noticed and the flask was immersed in an ice bath to maintain the reaction temperature at 21.5° C. to 25.5° C. for 2.1 hours. The reaction mixture was permitted to settle overnight. The acid layer was removed, washed once with 30 mL EDC, and discarded. The combined EDC solutions were quenched with 2% NaHCO3 (600 mL), washed with deionized water (400 mL), 1% NaHCO3 solution (400 mL), deionized water (400 mL, twice), and stripped in vacuo. The resulting light yellow liquid weighed 48.9 g (89.5% yield), and contained 1.8% EDC and 98.2% dl- and meso-(4,5-dichloromethyl)-1,3-dioxolane, as determined by GC analysis and proton NMR (CDCl3) δ (s, --OCH2O--), 4.1 (m, ClCH2CHCHCH2Cl), 3.6(d, ClCH2CHCHCH2Cl).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05698718uspto-grants-1997_12