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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177144Generated: October 27, 2026

Triethylborane → Methyl 3-(3-ethyl-4-hydroxyphenyl)propanoate

https://huagongshe.com/reaction/2177144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylboraneHCID 7357—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 3-(3-bromo-4-hydroxyphenyl)propanoateHCID 22558720—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(3-ethyl-4-hydroxyphenyl)propanoateHCID 90418287—

Reaction Conditions

Temperature65 °C

Reaction Steps

Into a 50-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed methyl 3-(3-bromo-4-hydroxyphenyl)propanoate (220 mg, 0.85 mmol, 1.00 equiv), Pd(dppf)Cl2 (25.76 mg, 0.04 mmol, 0.04 equiv), Cs2CO3 (616.4 mg), tetrahydrofuran (5 mL), triethylborane (1.26 mL). The resulting solution was stirred overnight at 65° C. in an oil bath. The reaction was then quenched by the addition of 5 mL of water. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with 20 mL of EA. The resulting mixture was washed with 3×10 mL of H2O. The mixture was dried over anhydrous sodium sulfate. The residue was applied onto a silica gel column with ethylacetate/petroleum ether (10:90). This resulted in 300 mg (170%) of methyl 3-(3-ethyl-4-hydroxyphenyl)propanoate as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-a5ce451417444c5caeb8f3921e094aef
Source noteuspto-grants-2015_06