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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589322Generated: October 30, 2026

6-Aminohexanoic Acid → 6-((Phenylsulphonyl)amino)hexanoic acid

https://huagongshe.com/reaction/589322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Aminohexanoic AcidHCID 564—
ReactantBenzenesulfonyl chlorideHCID 7369—
SolventSodium HydroxideHCID 14798—
Solvent1,4-DioxaneHCID 31275—
Product6-((Phenylsulphonyl)amino)hexanoic acidHCID 301727855%

Reaction Steps

Benzenesulfonyl chloride (2.5 ml, 19 mmol) was added to a solution of 6-aminohexanoic acid (1 g, 7.62 mmol) in 2N NaOH (22 ml) and dioxane (3 ml), while stirring at 0° C.-5° C. The mixture was allowed to warm to room temperature and stirred for 1 hour. The reaction mixture was washed with ethyl acetate (50 ml), then acidified to pH 2 with 37% hydrochloric acid and extracted with ethyl acetate (2×50 ml). The combined organic layers were dried over sodium sulfate and concentrated. The residue was triturated with hexane. The solid was collected by filtration and dried under vacuum at 50° C. affording 1.1 g of the title compound (55% yield). M.p. 113-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233115B2
Source datasetuspto-grants-2016_01
ORD IDord-d34639153f4340c8a9642bd6c33deda3
Source noteuspto-grants-2016_01