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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042613Generated: October 29, 2026

3,5-Dinitrobenzyl alcohol → HCID 58193600, compound

https://huagongshe.com/reaction/1042613

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 numberUS08557922B2
Source datasetuspto-grants-2013_10
ORD IDord-9c443ed807164627a2dc17b5056a71fa
Source noteuspto-grants-2013_10