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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502525Generated: October 29, 2026

Stannous Chloride → trans-4-Aminostilbene

https://huagongshe.com/reaction/1502525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
Reactanttrans-4-NitrostilbeneHCID 639659—
SolventAcetoneHCID 180—
SolventHydrochloric AcidHCID 313—
Producttrans-4-AminostilbeneHCID 1272788—

Reaction Steps

In an embodiment of the invention, a method for preparing the aforesaid alignment film in a laboratory level is illustrated as an example. 10 g of 4-nitrobenzyl bromide is mixed with 12 g of triphenylphosphine and dissolved in 150 ml of a dry tetrahydrofuran solution, heated to 75° C. and agitated under reflux for 48 hours, to obtain 8.2 g of a dry white p-nitrobenzyl triphenylphosphine. The p-nitrobenzyl triphenylphosphine is mixed with 2.6 g of p-nitrobenzaldehyde in a 150 ml tetrahydrofuran solution, and agitated under room temperature for about 24 hours to obtain 4.2 g of p-nitrostilbene. The resultant p-nitrostilbene is mixed with 14.7 g of tin dichloride, dissolved in a mixed solution of 30 ml/40% hydrochloride acid and 100 ml acetone, agitated under the room temperature for about 2 hours and refluxed for 8 hours to obtain p-aminostilbene. The p-aminostilbene is mixed with 9,9′-bianthracyl tetracarboxylic dianhydride in a dry NMP (N-methyl-pyrrolidone) solution under agitation for 24 hours, under protection of nitrogen gas, to obtain the precursor of the polyimide alignment film involved in the embodiment. The precursor is heated to 230° C. to obtain the final alignment film, which is a light sensitive alignment film.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09207497B2
Source datasetuspto-grants-2015_12
ORD IDord-cbda2561fb2747ae83209fccde494215
Source noteuspto-grants-2015_12