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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192761Generated: November 3, 2026

Methanol → HCID 86640905, compound

https://huagongshe.com/reaction/2192761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
Reactant4-Methoxy cinnamic acidHCID 13245—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
SolventDimethylformamideHCID 6228—
ProductHCID 86640905HCID 86640905—
ProductHCID 86640906HCID 86640906—

Reaction Steps

The 5-norbornene-2-methanol/ethylene copolymer (18.4 g, 0.121 mol) that was polymerized in (2), 4-methoxy cinnamic acid (Aldrich, 21.5 g, 0.121 mol), EDC [1-(3-dimethylaminopropyl)-3-ethylcarboimide hydrochloride] (Aldrich, 37 g, 0.194 mol), and HOBT (1-hydroxybenzotriazole hydrate) (Aldrich, 24.5 g, 0.182 mol) were put into the 2-neck flask having the volume of 250 ml, and then dissolved in 100 ml of DMF. After the temperature was reduced to 0° C., triethylamine (Aldrich, 75 ml, 0.605 mol) was slowly dropped on the reaction solution. After the temperature was increased to normal temperature and maintained for 3 hours, when the reaction was finished, the reaction solution was dropped on a large amount of methanol to precipitate the polymer, and the polymer was filtered to obtain the 5-norbornene-2-methyl-(4-methoxy cinnamate)/ethylene copolymer to which the 4-methoxy cinnamoyl functional group was introduced (yield: 90.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329841B2
Source datasetuspto-grants-2012_12
ORD IDord-7ed2a3ca1a5f433f9f60c3afc76329bb
Source noteuspto-grants-2012_12