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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059808Generated: November 1, 2026

2-Propenoic acid, 3-phenyl-, methyl ester → HCID 15941322, compound

https://huagongshe.com/reaction/2059808

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propenoic acid, 3-phenyl-, methyl esterHCID 7644—
ReactantLithium diisopropylamideHCID 2724682—
ReactantN,N-Di(propan-2-yl)-2-(pyridin-3-yl)acetamideHCID 57429229—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15941322HCID 15941322—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) solution of N,N-diisopropyl-2-pyridin-3-ylacetamide (740 mg, 3.36 mmol) in dry THF (30 mL) was added a solution of LDA (1.5 M) in THF (4.5 mL, 6.72 mmol). The reaction mixture was stirred at 0° C. for 30 min and then cooled to −78° C. Solid methyl cinnamate (654 mg, 4.031 mmol) was added in one portion. The cooling bath was removed and the reaction mixture was allowed to warm up to room temperature. After 1.5 h, the reaction was quenched by adding a saturated aqueous solution of NH4Cl and partitioned between CH2Cl2 and saturated aqueous NaHCO3. The aqueous layer was extracted with CH2Cl2 (3×). The combined organic layers were dried over anhydrous Na2SO4 and concentrated. The resulting red viscous liquid was purified by flash chromatography using a linear gradient of 0% to 5% MeOH—NH3 (90:10 v/v) in CH2Cl2. Yellow solid, single diastereomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278317B2
Source datasetuspto-grants-2012_10
ORD IDord-b2ac23d0660e43dd968d208c572aa537
Source noteuspto-grants-2012_10