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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193508Generated: November 3, 2026

3,5-Dinitrobenzyl alcohol → HCID 58193600, compound

https://huagongshe.com/reaction/2193508

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dinitrobenzyl alcoholHCID 116978—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 59850420HCID 59850420—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 58193600HCID 581936007.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.00 g (51.0 mmol) of 3,5-dinitrobenzylalcohol, 2.00 g (51.0 mmol) of (2E)-3-(4-{[4-(4,4,4-trifluorobutoxy)benzoyl]oxy}phenyl)acrylic acid, 62 mg (0.51 mmol) of 4-Dimethylaminopyridine are dissolved in 10 ml of dichloromethane. 1.07 g (56.0 mmol) of N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC hydrochloride) are added at 0° C. The solution is stirred for 1 h at 0° C. and allowed to stir at room temperature overnight. After 22 hours at room temperature the reaction mixture is partitioned between dichloromethane and water. The organic phase is washed repeatedly with water, dried over sodium sulphate, filtered and concentrated by rotary evaporation to yield 3,5-dinitrobenzyl (2E)3-{4-[(4-(4,4,4-trifluorobutoxy)benzoyl)oxy]phenyl}acrylate 2.1 g as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329823B2
Source datasetuspto-grants-2012_12
ORD IDord-ca331607af8149eb98bd6748a55bff8f
Source noteuspto-grants-2012_12