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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726128Generated: November 2, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 68973628, compound

https://huagongshe.com/reaction/1726128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant4-bromo-N-methylbenzene-1-sulfonamideHCID 101215—
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68973628HCID 6897362841%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-bromo-N-methyl-benzenesulfonamide (Marvel; Smith, J. Am. Chem. Soc., 45, 1923, 2697) (1.00 g, 4.00 mmol) in THF (35 mL) at −78° C. was added MeLi (4.00 mmol) and the solution was stirred at −78° C. for 15 minutes. n-BuLi (1.95M in hexanes, 2.05 mL, 4.00 mmol) was then added. After the solution was stirred at −78° C. for 45 minutes, TMEDA (1.20 mL, 8.00 mmol) was added followed by a solution of 4-formyl-piperidine-1-carboxylic acid tert-butyl ester (4.76 g, 22.30 mmol) in THF (5 mL), and the mixture was stirred at −78° C. for 1 hour. Work-up and purification gave 4-[hydroxy-(4-methylsulfamoyl-phenyl)-methyl]-piperidine-1-carboxylic acid tert-butyl ester (622 mg, 41%) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491735B2
Source datasetuspto-grants-2009_02
ORD IDord-5b829721853d451db835824e1311c700
Source noteuspto-grants-2009_02