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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797005Generated: October 29, 2026

Benzenesulfonyl chloride → HCID 178525721, compound

https://huagongshe.com/reaction/1797005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178511262HCID 178511262—
SolventWaterHCID 962—
ProductHCID 178525721HCID 178525721—

Reaction Steps

trans-4-(Aminomethyl)cyclohexane carboxylic acid (15.2 g, 0.097 mol) was dissolved in a 2N NaOH solution (96.5 mL, 2 equivalents). The solution was brought to 10° C., benzenesulfonyl chloride (17.1 g, 0.097 mol) was added dropwise and then the mixture was stirred overnight at room temperature. The mixture was diluted with water, the solution was washed with ether, and then the aqueous portion was acidified with 12N HCl to give an oily precipitate. The precipitate was extracted with CH2Cl2, and the extracts were dried (Na2SO4) and concentrated under reduced pressure to give trans-4-(Benzenesulfonylamino-methyl)-cyclohexanecarboxylic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034034B2
Source datasetuspto-grants-2006_04
ORD IDord-dd76f585c566482484e2705ec56cf2b1
Source noteuspto-grants-2006_04