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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486227Generated: October 26, 2026

Azobisisobutyronitrile → Butyl 3-(2-(2-oxo-1,3-dioxolan-4-yl)ethylthio)propanoate

https://huagongshe.com/reaction/1486227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantButyl 3-mercaptopropionateHCID 85335—
Reactant1,3-Dioxolan-2-one, 4-ethenyl-HCID 2735038—
ProductButyl 3-(2-(2-oxo-1,3-dioxolan-4-yl)ethylthio)propanoateHCID 118389509—

Reaction Conditions

Temperature110 °C

Reaction Steps

3.87 grams (33.9 mmol, MW: 114.10) 4-vinyl-1,3-dioxaolane-2-one, 5.0 grams (30.8 mol, MW: 162.25) butyl-3-mercaptopropionate and 0.505 grams (3.1 mmol, MW: 164.21) 2,2′-azobis(2-methylpropionitrile) (AIBN) were charged in a 25 milliliter thick sealed glass reactor. After addition, the reaction mixture was stirred for 22 hours at 110° C. The reaction was then stopped and cooled down to room temperature. The excess of unreacted 4-vinyl-1,3-dioxaolane-2-one was removed by air bath oven at 180° C. under vacuum for 1 hour. The final product was determined by IR, 13CNMR. Yield: 4.26 grams (50%). IR: (cm−1) 2960, 2933, 2873, 1803, 1731, 1456, 1390, 1351, 1246, 1169, 1065, 772. 13C NMR (CDCl3): 171.7, 154.7, 124.6, 113.4, 75.4, 69.2, 64.5, 35.0, 33.9, 30.5, 27.2, 19.1, 13.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422502B2
Source datasetuspto-grants-2016_08
ORD IDord-1f0ecbfcecb34a16a3d0654fc8db0d59
Source noteuspto-grants-2016_08