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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Iodobenzyl alcoholHCID 42300—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
Product(E)-3-(3-Hydroxymethyl-phenyl)-acrylic acid methyl esterHCID 5979468897%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732443B2
Source datasetuspto-grants-2010_06
ORD IDord-a51aab874b354bb2a3c422fc2effc228
Source noteuspto-grants-2010_06