Thionyl Chloride → HCID 22026129, compound

Temperature

85 °C

4-(Ethoxycarbonyl)-5,6-dihydro-2H-pyran-3-sulfonic acid (27.5 g) was dissolved in thionyl chloride (82.6 ml) and the mixture was stirred at room temperature→85° C. for 3 h. The reaction mixture was concentrated to dryness under reduced pressure and the residue was dissolved in ethyl acetate (100 ml). The obtained solution was partitioned by adding diluted brine (120 ml). The ethyl acetate layer was washed twice with saturated brine (50 ml) and dried over anhydrous sodium sulfate. The solvent was evaporated and the obtained residue was purified by silica gel column chromatography (eluent:ethyl acetate/hexane=1/7→1/5). The objective product was concentrated under reduced pressure and the crystals produced by freezing were washed with hexane to give ethyl 5-(chlorosulfonyl)-3,6-dihydro-2H-pyran-4-carboxylate (7.81 g) as pale-yellow crystals.

1. concentrationThe reaction mixture was concentrated to dryness under reduced pressure
2. dissolutionthe residue was dissolved in ethyl acetate (100 ml)
3. customThe obtained solution was partitioned
4. additionby adding diluted brine (120 ml)
5. washThe ethyl acetate layer was washed twice with saturated brine (50 ml)
6. dry with materialdried over anhydrous sodium sulfate
7. customThe solvent was evaporated
8. customthe obtained residue was purified by silica gel column chromatography (eluent:ethyl acetate/hexane=1/7→1/5)
9. concentrationThe objective product was concentrated under reduced pressure
10. customthe crystals produced by freezing
11. washwere washed with hexane

ORD record

ord-d9c5cd1e676e42a9b7e77cf9e1fd14c7

Source dataset

uspto-grants-2008_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07417059B2