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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477629Generated: November 2, 2026

Toluene → HCID 117849010, compound

https://huagongshe.com/reaction/1477629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriethyl(methoxycarbonylsulfamoyl)aminiumHCID 2724995—
ReactantHCID 117848973HCID 117848973—
SolventEthyl AcetateHCID 8857—
ProductHCID 117849010HCID 11784901075%

Reaction Steps

To a toluene solution (40 mL) of tert-butyl (3S,4S)-4-(4-fluorophenyl)-4-hydroxy-3-(pivaloyloxy)piperidine-1-carboxylate (2.07 g, 5.23 mmol) synthesized in Reference Synthesis Example 130, methyl N-(triethylammoniosulfonyl)carbamate (1.74 g, 7.32 mmol) was added and the resultant mixture was stirred at 60° C. for 3 hours. After completion of the reaction, ethyl acetate was added to the reaction solution and the resultant mixture was washed with each of saturated sodium bicarbonate aqueous solution and saturated sodium chloride aqueous solution. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=9/1→3/1) to obtain the title compound (1.47 g, yield 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-ac9708de0ac44a52a0d3c655bf33d8e8
Source noteuspto-grants-2016_08