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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250103Generated: November 1, 2026

3-Hydroxybenzaldehyde → Methyl 3-Coumarate

https://huagongshe.com/reaction/1250103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantTrimethyl phosphonoacetateHCID 80029—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantLithium ChlorideHCID 433294—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-CoumarateHCID 535291086.4%

Reaction Steps

A solution of trimethyl phosphonoacetate (9.94 mL, 61.4 mmol), lithium chloride (2.60 g, 12.2 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (15.92 mL, 106.5 mmol) in acetonitrile (80 mL) at room temperature under a nitrogen atmosphere was stirred at room temperature for 30 minutes. 3-Hydroxybenzaldehyde (5.00 g, 40.9 mmol) was added, and the mixture was stirred at room temperature for an additional 3 hours. Water was added and the aqueous phase was extracted with diethyl ether. The combined organic fractions were washed with water, brine, dried over magnesium sulfate, and evaporated to dryness. Purification by flash chromatography, eluting with hexane/ethyl acetate, gave trans-3-(3-hydroxyphenyl)acrylic acid methyl ester as a white crystalline solid (6.30 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335459B1
Source datasetuspto-grants-2002_01
ORD IDord-18f601cb29d44ef3a14088d63952d063
Source noteuspto-grants-2002_01