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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748693Generated: October 30, 2026

2-Ethylhexylamine → HCID 86686308, compound

https://huagongshe.com/reaction/1748693

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-EthylhexylamineHCID 7719—
ReactantBis(2-ethylhexyl) ItaconateHCID 261108—
ProductHCID 86686308HCID 86686308—

Reaction Conditions

Temperature45 °C

Reaction Steps

Bis(2-ethylhexyl)itaconate (400 g; 1.13 Mol) was charged to a 1 L reaction vessel and the material stirred mechanically under nitrogen while heating to 45° C. 2-Ethylhexylamine (1.02 equiv.: 1.15 Mol; 148.7 g) was charged to a pressure-equalizing addition funnel and the amine added dropwise to the stirred diester over the course of one hour. During the addition, a moderate exotherm was observed and the mixture was allowed to heat to 70° C. When the addition was complete, the mixture was heated to 75° C. and held for one hour before cooling to room temperature overnight. The following day, the vessel was equipped with a distillation sidearm/condenser and heated to 120 to 125° C. under reduced pressure (−30″ Hg) (−762 mm) in order to remove 2-ethylhexanol and excess amine. When stripping was complete, the apparatus was backfilled with nitrogen and cooled to room temperature. The amount of 2-ethylhexanol collected was 141.7 g (1.09 Mol; 96.5% of theoretical recovery). The stripped product was warmed to 50° C. and filtered through a 1″ (2.5 cm) plug of silica gel, giving the final product as a light yellow liquid. H-NMR analysis of the product was consistent with the expected product. Sample materials were collected from this preparation and designated 1-(2-ethylhexyl)-5-oxo-3-pyrrolidinecarboxylic acid 2-ethylhexyl ester for comparison testing described in the Examples below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150740B2
Source datasetuspto-grants-2015_10
ORD IDord-6a3b3d03d16946d4aa5c6d1d2e66ebd8
Source noteuspto-grants-2015_10