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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35797Generated: October 26, 2026

6-Aminohexanoic Acid → 6-(cis-1,2,3,6-Tetrahydrophthalimido)hexanoic acid

https://huagongshe.com/reaction/35797

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Aminohexanoic AcidHCID 564—
ReactantTetrahydrophthalic anhydride, cis-HCID 98495—
SolventAcetic AcidHCID 176—
Product6-(cis-1,2,3,6-Tetrahydrophthalimido)hexanoic acidHCID 1551668—

Reaction Conditions

Temperature4 °C

Reaction Steps

31 g (0.2 mole) of cis-1,2,3,6-tetrahydrophthalic anhydride and 26.2 g (0.2 mole) of 6-aminohexanoic acid are dissolved in 400 ml. of acetic acid and warmed 3 hours on a steam bath. The cooled solution is concentrated to remove most of the acetic acid and the residue taken up in 200 ml. of methylene chloride. The solution is washed twice with water and dried over sodium sulfate. The solvent is removed and the residue taken up in 500 ml toluene. Para-toluenesulfonic acid (1 g) is added to the solution, followed by reflux for 10 hrs. with a Dean-Stark water trap. The solution is cooled and concentrated to about 50 ml and diluted with 50 ml of hexane. The mixture is shaken for a few minutes until the oil crystallizes then cooled at 4° C. for several hours, filtered and dried at 50° C. The light yellow crystals (32 g) are taken up in chloroform and filtered to remove any precipitate. The solution is diluted with hexane near the cloud point, cooled until a crystalline mass accumulates, filtered and dried to yield white crystals, m.p. 85°-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411869
Source datasetuspto-grants-1995_05
ORD IDord-8ae8e440dc58469e85ec63cb2158cff9
Source noteuspto-grants-1995_05