HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64421Generated: October 28, 2026
Triethylamine → tert-butyl (2E)-3-[2-(hydroxymethyl)-4-methylphenyl]acrylate
https://huagongshe.com/reaction/64421
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | (2-Bromo-5-methylphenyl)methanol | HCID 54173415 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-butyl (2E)-3-[2-(hydroxymethyl)-4-methylphenyl]acrylate | HCID 86713430 | — |
Reaction Steps
A mixture of 2.64 g of (2-bromo-5-methylphenyl)methanol, 246 mg of bis(dibenzylideneacetone)palladium, 2.95 ml of tert-butylacrylate, 442 mg of tris(2-methylphenyl)phosphine, 2.5 ml of triethylamine, and 24 ml of DMF was stirred at 100° C. for 24 hours. After leaving to be cooled at room temperature, water and ethyl acetate were added thereto to carry out a layer separation operation. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 2.32 g of tert-butyl (2E)-3-[2-(hydroxymethyl)-4-methylphenyl]acrylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447090B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-889565f5456a4cd5a1a167f7cafd3cb8 |
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| Source note | uspto-grants-2016_09 |
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