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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429610Generated: October 25, 2026

N,N-Dimethylglycine → trans-Stilbene

https://huagongshe.com/reaction/429610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
ReactantStyreneHCID 7501—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium AcetateHCID 517045—
CatalystTetraphenylphosphonium ChlorideHCID 164911—
SolventDiethyl EtherHCID 3283—
Product1,1-DiphenylethyleneHCID 10740—
Producttrans-StilbeneHCID 63808897.4%
Productcis-StilbeneHCID 53567850.6%

Reaction Steps

To a reaction vessel standing on a scale which is sealed with a septum cap, 5.3 mg (0.02 mmol) of (CH3CN)2PdCl2, 45 mg (0.12 mmol) of Ph4PCl and 12.4 mg (0.12 mmol) of dimethylglycine are added, followed by two cycles of evacuation and flushing with argon. Under argon, 657.7 mg (8 mmol) of anhydrous sodium acetate and 1 ml of NMP are added. 452 mg (4.01 mmol) of Cl-benzene and 636 mg (6.11 mmol) of styrene is mixed with 1 ml of NMP and added dropwise in 6 portions within 6 hours, the first portion being added at room temperature and the others at 140° C. Stirring is performed at 140° C. for a total of 24 h. According to the processing described in Example 1 using 10 ml of diethyl ether, a 64.2% yield of Heck products (97.4% trans-stilbene, 0.6% cis-stilbene, and 2.0%- 1,1-diphenylethene) is obtained with 76.6% conversion of Cl-benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316675B1
Source datasetuspto-grants-2001_11
ORD IDord-d92d3569a6cc478798316003861e97d6
Source noteuspto-grants-2001_11