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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dinitrobenzyl alcohol | HCID 116978 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 59850420 | HCID 59850420 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58193600 | HCID 58193600 | 7.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557922B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-9c443ed807164627a2dc17b5056a71fa |
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| Source note | uspto-grants-2013_10 |
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