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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848884Generated: November 2, 2026

Hydrochloric Acid → HCID 178514755, compound

https://huagongshe.com/reaction/1848884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactantcis-4-(tert-Butoxycarbonylamino)cyclohexanolHCID 1514287—
Reactant4-Fluoro-3-nitrobenzenesulfonamideHCID 16782487—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178514755HCID 178514755—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of tert-butyl 4-hydroxycyclohexylcarbamate (0.250 g) in tetrahydrofuran (5 mL) was added sodium hydride (0.186 g). After stirring for 15 minutes, 4-fluoro-3-nitrobenzenesulfonamide (0.256 g) was added as a solution in tetrahydrofuran (1 mL). The reaction was heated to 60° C. for 1.5 hours, cooled and poured into a mixture of dichloromethane (100 mL) and water (25 mL). The aqueous layer was adjusted to pH˜4 with 1N aqueous HCl and the organic layer was separated, washed with brine (50 mL), dried over magnesium sulfate and concentrated. The residue was loaded onto silica gel (GraceResolv 40 g) and eluted using a gradient of 0.5% to 7.5% methanol/dichloromethane over 30 minutes. This solid was immediately treated with HCl (4.0M in dioxane, 5 mL) at room temperature for 1 hours and concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952157B2
Source datasetuspto-grants-2015_02
ORD IDord-353a71d1f44e44399511495266353573
Source noteuspto-grants-2015_02