HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15005Generated: October 26, 2026
Methyl Acrylate → (E)-3-(3-Hydroxymethyl-phenyl)-acrylic acid methyl ester
https://huagongshe.com/reaction/15005
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Iodobenzyl alcohol | HCID 42300 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (E)-3-(3-Hydroxymethyl-phenyl)-acrylic acid methyl ester | HCID 59794688 | 97% |
Reaction Steps
The procedure described in Reich, S. H. etal. J. Med. Chem. 2000, 43, 1670 was followed. Pd(OAc)2 (8.2 mg, 0.037 mmol) and triethylamine (0.360 mL, 2.58 mmol) were added to a solution of 3-iodobenzyl alcohol 15 (0.27 mL, 2.13 mmol) and methyl acrylate 16 (0.220 mL, 2.44 mmol) in CH3CN (4.5 mL). The reaction vessel was sealed with a Teflon screw-cap and was heated at 100° C. for 5 h. At this time, the reaction was allowed to cool to room temperature and the tube was charged with 0.22 mL more of methyl acrylate, 11.7 mg Pd(OAc)2 and 0.360 mL triethylamine. The reaction was heated at 100° C. overnight and then 10 mL saturated ammonium chloride solution was added. The resulting mixture was extracted with dichloromethane (3×40 mL) and the combined dichloromethane solution was dried (Na2SO4), filtered and evaporated. Purification by flash chromatography on silica gel (30% ethyl acetate/hexanes) gave 395 mg (97%) of compound 17.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732443B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-a51aab874b354bb2a3c422fc2effc228 |
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| Source note | uspto-grants-2010_06 |
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