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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | Di-tert-butylphenylphosphine | HCID 316378 | — |
| Reactant | alpha-Cyclohexylcyclohexanemethanamine | HCID 10774245 | — |
| Reactant | 4-Chloro-2-methyl-1-(trifluoromethyl)benzene | HCID 12712338 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Methyl 3-methyl-4-trifluoromethylcinnamate | HCID 69642322 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07102046B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-9d64549484ee408c94529c667c2bd8de |
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| Source note | uspto-grants-2006_09 |
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