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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537820Generated: October 29, 2026

1,2-Dichloroethane → HCID 59294727, compound

https://huagongshe.com/reaction/537820

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Dimethylamino)butyric acid hydrochlorideHCID 12691640—
ReactantHCID 58205088HCID 58205088—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 59294727HCID 5929472787.3%

Reaction Steps

To a solution of diphytanyl methanol (6.4 g, 10.3 mmol) and 4-(dimethylamino) butyric acid hydrochloride (2.25 g, 13.4 mmol) in anhydrous dichloromethane (60 mL) under nitrogen at room temperature was added EDC (2.77 g, 18.0 mmol), diisopropylethylamine (5.4 mL, 31.0 mmol), and 4-dimethylaminopyridine (45 mg, 0.37 mmol). After 16 hours the reaction mixture was diluted with dichloromethane (75 mL). The organic layer was washed with saturated NaHCO3, water, and brine, and then dried on MgSO4, filtered, and concentrated. The resulting yellow oil was purified by column chromatography (column 10″L×2″W; eluted with a gradient of 100% hexanes→10%→50% ethyl acetate in hexanes) to afford the product as a pale yellow oil (3.53 g, 49%) with recovery of some phytanyl methanol (2.81 g, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865675B2
Source datasetuspto-grants-2014_10
ORD IDord-1ed799a2c35548d097135e60f805649e
Source noteuspto-grants-2014_10