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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601743Generated: October 31, 2026

4-Methoxybenzenesulfonyl chloride → (trans)-2-(4-Methoxybenzenesulfonyl)aminocyclohexanecarboxylic acid

https://huagongshe.com/reaction/1601743

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantTriethylamineHCID 8471—
Reactanttrans-2-Aminocyclohexanecarboxylic acidHCID 2724640—
SolventPentaneHCID 8003—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product(trans)-2-(4-Methoxybenzenesulfonyl)aminocyclohexanecarboxylic acidHCID 1543059252.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a room temperature solution of 1 g (6.8 mmol) of trans-2-amino-1-cyclohexylcarboxylic acid in 50 ml of dioxane:H2O (1:1) containing 1.7 ml (12.2 mmol) of triethylamine was added 1.54 g (7.46 mmol) of 4-methoxybenzenesulfonyl chloride. The mixture was stirred at 25° C. for 18 h. The resulting mixture was diluted with pentane to afford 1.119 g (51%) of the desired sulfonamide product as a white solid. 1H NMR(DMSO-d6): 7.7 ppm (dd, 2H, Ar), 7.4 ppm (d, 1H, NH), 7.0 ppm (dd, 2H, Ar), 3.8 ppm (s, 3H, OMe), 3.5 ppm (m, 1H, N--CH), 1.0-1.7 ppm (m, 9H, hydrocarbon).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977408
Source datasetuspto-grants-1999_11
ORD IDord-af5e709f086e495c9fbb998992ad85e3
Source noteuspto-grants-1999_11