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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212640Generated: October 25, 2026

Methyl Acrylate → Methyl 3-methyl-4-trifluoromethylcinnamate

https://huagongshe.com/reaction/2212640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantDi-tert-butylphenylphosphineHCID 316378—
Reactantalpha-CyclohexylcyclohexanemethanamineHCID 10774245—
Reactant4-Chloro-2-methyl-1-(trifluoromethyl)benzeneHCID 12712338—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductMethyl 3-methyl-4-trifluoromethylcinnamateHCID 6964232286%

Reaction Steps

0.619 g (7.2 mmol) of methyl acrylate, 38.7 mg (120 μmol) of NBu4Br, 6.7 mg (30 μmol) of palladium acetate and 26.7 mg (120 μmol) of phenyldi(t-butyl)phosphine are weighed into a Schlenk vessel. 1.17 g (6 mmol) of 3-methyl-4-trifluoromethylchlorobenzene and 1.53 ml (7.2 mmol) of dicyclohexylmethylamine and also 3.5 ml of dimethylacetamide are then added. The Schlenk vessel is placed in a heating bath at 130° C. and the contents are stirred. After 4 hours, the contents are poured into 30 ml of water and the product is extracted by shaking with t-butyl methyl ether. After drying the organic phase over MgSO4, the solvent is removed under reduced pressure and the product is isolated. Yellowish, crystalline solid. Yield: 86%, two products in a ratio of 99:1 (trans/cis products).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07102046B2
Source datasetuspto-grants-2006_09
ORD IDord-9d64549484ee408c94529c667c2bd8de
Source noteuspto-grants-2006_09