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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019476Generated: November 1, 2026

1-Butanol → HCID 131731368, compound

https://huagongshe.com/reaction/1019476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMaleic AnhydrideHCID 7923—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86613229HCID 86613229—
SolventEthyl AcetateHCID 8857—
ProductHCID 131731368HCID 131731368—

Reaction Conditions

Temperature60 °C

Reaction Steps

Maleic Anhydride (MA, 19.6 g, 200.0 mmol), Phenyl Ethyl Norbornene (PENB, 39.6 g, 200 mmol) and AIBN (3.3 g, 20.0 mmol) was dissolved in EtOAc (36.2 g) and charged to an appropriately sized reaction vessel. The solution was sparged with nitrogen for 10 min to remove oxygen and then heated to 60° C. The mixture was allowed to stir at 60° C., for 20 hr. The reaction mixture was concentrated in vacuo and redissolved in THF (20 wt %). The resulting solution was added to the suspension of NaOH (8.80 g, 220 mmol), BuOH (74.12 g, 1 mol) and TI-IF (74.12 g) which were mixed at 70° C. for 1 hr. The mixture was allowed to stir for 2 hr at 70° C. and then was cooled to room temperature. The reaction mixture was treated with cone. HClacq for protonation, and then washed three times to remove residual salts and acid. The organic phase was separated and then concentrated in vacuo, redissolved in THF to form an approximately 20 wt % copolymer solution and then the copolymer was precipitated by adding the THF solution to hexane (20 fold excess). The copolymer was separated by filtration and dried in a vacuum oven at 80° C. for 16 hr. Approximately, 37.5 g (51%) of the ROMA copolymer of MA/PENB with BuOH was isolated (GPC Mw=9,900 Mn=5,400).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08715900B2
Source datasetuspto-grants-2014_05
ORD IDord-3f83889be3314269a86fcb65a87f3a66
Source noteuspto-grants-2014_05