Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78689Generated: October 25, 2026

Succinic anhydride → HCID 86624398, compound

https://huagongshe.com/reaction/78689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinic anhydrideHCID 7922—
ReactantEthyl 3-mercaptopropionateHCID 21625—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrile pyridineHCID 21959178—
ProductHCID 86624398HCID 86624398—

Reaction Steps

As shown in FIG. 2, Ethyl 3-mercaptopropionate (2.95 g, 22 mmol) was added under argon to a stirring solution of succinic anhydride (2.0 g, 20 mmol) and DMAP (122 mg, 1 mmol) in 25 ml of acetonitrile-pyridine (9:1). The reaction mixture was stirred at room temperature overnight. The solution was concentrated under reduced pressure and dried in vacuo. The residue was dissolved in 50 ml of EtOAc. The EtOAc solution was washed with 0.1 N HCl aqueous solution 30 ml×3, H2O×3, dried over anhydrous MgSO4. After filtration, the solution was concentrated to dry under reduced pressure and in vacuo. 1H NMR (CDCl3, 500 MHz) δ 10.23 (s, br), 4.14 (2H, q, J=7.0 Hz, —CH2—CH3), 3.13 (2H, t, J=7.0 Hz, —S—CH2—), 2.88 (2H, t, J=7.0 Hz, —S—CO—CH2—), 2.69 (2H, t, J=7.0 Hz, —S—CH2—CH2—), 2.62 (2H, t, J=7.0 Hz, —CH2—COOH), 1.25 (3H, t, J=7.0 Hz, —CH2—CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841408B2
Source datasetuspto-grants-2014_09
ORD IDord-ba250d95f261483b8ef9cdf2da8c3578
Source noteuspto-grants-2014_09