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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177482Generated: October 29, 2026

Diisopropylamine → HCID 59438430, compound

https://huagongshe.com/reaction/2177482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantHCID 59438516HCID 59438516—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 59438430HCID 5943843054%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 78.4 ul (0.555 mmol) diisopropylamine in 2 ml THF were added 347 ul (0.555 mmol) of a 1.6M n-BuLi solution in hexane at −5° C. The solution was stirred for 15 minutes at 0° C. and then cooled to −70° C. A solution of 100 mg (0.427 mmol) rac-1-methyl-5-nitro-5-phenyl-piperidin-2-one in 1 ml THF was added dropwise. The brown solution was stirred at −70° C. for 45 minutes. A solution of 180 mg (0.555 mmol) N-fluorobenzenesulphonimide in 1 ml THF was added dropwise. The mixture was stirred at −70° C. for 1.5 hour, quenched with 2 ml of a 20% NH4Cl solution and allowed to warm to room temperature. Water and ethyl acetate were added. The aqueous layer was extracted twice with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The crude oil was purified on silica gel (Eluent: Heptane/ethyl acetate 0 to 100%) to provide 58 mg (54%) of the title compound as a light yellow solid. MS (m/e): 253.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067911B2
Source datasetuspto-grants-2015_06
ORD IDord-eaad55ce081a4affb711ba6e7b1757dc
Source noteuspto-grants-2015_06