HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026366Generated: October 29, 2026
N,N'-Diphenyl-P-Phenylenediamine → HCID 66643440, compound
https://huagongshe.com/reaction/1026366
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N'-Diphenyl-P-Phenylenediamine | HCID 6319 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | HCID 10888853 | HCID 10888853 | — |
| Product | HCID 66643440 | HCID 66643440 | — |
Reaction Steps
Into a 3-neck round-bottomed flask was placed (in order): N,N′-diphenyl-1,4-phenylenediamine (0.53 g, 2.04×10−3 moles), 3-Methyl-3-(phenylthio)butan-1-ol (50.0 g, 0.255 moles) and ethyl acrylate (276 mL, 2.55 moles). The apparatus was then assembled for reactive distillation through a Claisen head and purge-filled with nitrogen gas. The reaction flask was heated to 110-115° C. and after ca. 5 mL of ethyl acrylate had distilled over, titanium(IV) isoproproxide (TPT, 2.26 mL, 7.65×10−3 moles) was added to the reaction mixture via syringe in one portion. The rate of distillation immediately increased significantly and the distillate vapour temperature decreased from 99° C. to 90° C. These distillation conditions were maintained for a period of 150 minutes before the apparatus was evacuated by means of a 10 mbar PTFE-diaphragm pump and the remaining ethyl acrylate was stripped from the reaction mixture. The apparatus was then pumped down using a two-stage oil pump and the crude product distilled over at a vapour temperature of 109.5-112° C. (0.18 Torr, appearance: golden liquid, yield: 50.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729203B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-37329e03f2674494a13a1925ff33211e |
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| Source note | uspto-grants-2014_05 |
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