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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602745Generated: October 26, 2026

Water → HCID 67266827, compound

https://huagongshe.com/reaction/602745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantBenzenesulfonyl-(3-oxo-cyclohexyl)-acetic acid methyl esterHCID 11088194—
SolventDimethylformamideHCID 6228—
ProductHCID 67266827HCID 6726682729.1%

Reaction Steps

To a stirred solution of 10 g (0.032 mol) of benzenesulfonyl-(3-oxo-cyclohexyl)-acetic acid methyl ester in 110 mL of DMF at 0° C., 1.42 g (0.035 mol, 1.1 eq) of NaH (60%) were added. The reaction mixture was stirred at this temperature for one hour, and 15.71 g (0.048 mol, 1.5 eq) of N-fluorobenzenesulfonimide were added. After 2 hours at RT, the reaction mixture was poured into water and extracted with EtOAc. The combined organic phases were dried over Na2SO4, filtered and evaporated. The resulting two diastereomers were separated by column chromatography on silica gel with heptane/EtOAc 2:1, yielding 3.06 g (27%) of (RS,SR)-benzenesulfonyl-fluoro-(3-oxo-cyclohexyl)-acetic acid methyl ester as a white solid, MS: 329 (MH+) and 3.2 g (28%) of (RR,SS)-benzenesulfonyl-fluoro-(3-oxo-cyclohexyl)-acetic acid methyl ester as a white solid, MS: 329 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906546B2
Source datasetuspto-grants-2011_03
ORD IDord-8ca6bfc6e5ac4592988b2d1816b7b3e8
Source noteuspto-grants-2011_03