Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191164Generated: October 26, 2026

1,4-Butanediol → Ethyl 3-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-7,12-dioxaspiro[5.6]dodec-1-ene-2-carboxylate

https://huagongshe.com/reaction/2191164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-ButanediolHCID 8064—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantTrimethyl(1-methylethoxy)silaneHCID 74578—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylateHCID 67192731—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-7,12-dioxaspiro[5.6]dodec-1-ene-2-carboxylateHCID 578709693%

Reaction Steps

34 mg (0.61 mmol) of 1,4-butanediol was dissolved in 5 ml of dichloromethane, 0.32 ml (1.83 mmol) of isopropoxytrimethylsilane, and 200 mg (0.47 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylate obtained in Example (16a) and 4 μl (0.024 mmol) of trimethylsilyl trifluoromethanesulfonate were sequentially added thereto with stirring under ice-cooling, followed by stirring for 2 hours at the same temperature. Saturated aqueous sodium hydrogencarbonate was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=3:1), and the resulting solid was further washed with hexane to give 6 mg of the title compound as a white powder (yield: 3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE043858E1
Source datasetuspto-grants-2012_12
ORD IDord-2e134733c4294b8d952611a9e4548ce8
Source noteuspto-grants-2012_12