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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47791Generated: October 30, 2026

Sodium hydride → 3-{4-[2-(Tert-butoxycarbonyl-heptyl-amino)-ethyl]-phenyl}-2-ethoxy-acrylic acid ethyl ester

https://huagongshe.com/reaction/47791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Diphenylphosphinoyl-2-ethoxyacetic acid ethyl esterHCID 57438376—
Reactant[2-(4-Formyl-phenyl)-ethyl]-heptyl-carbamic acid tert-butyl esterHCID 86586368—
SolventTetrahydrofuranHCID 8028—
Product3-{4-[2-(Tert-butoxycarbonyl-heptyl-amino)-ethyl]-phenyl}-2-ethoxy-acrylic acid ethyl esterHCID 6988467144%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 60% by weight sodium hydride oil dispersion (6.97 mmol, 277 mg) in anhydrous tetrahydrofuran (20 mL) cooled to 0° C. was added 2-diphenylphosphinoyl-2-ethoxyacetic acid ethyl ester (3.80 mmol, 1.26 g) followed by [2-(4-formyl-phenyl)-ethyl]-heptyl-carbamic acid tert-butyl ester (3.46 mmol, 1.2 g) dissolved in anhydrous tetrahydrofuran (15 mL). The resulting heterogeneous solution was heated to reflux for one hour. The mixture was cooled to room temperature, quenched by the addition of ethanol (2 mL) and diluted with water (20 mL). The aqueous layer was isolated and extracted with diethyl ether (3×). The organic layers were combined, washed with saturated NaHCO3 (2×), brine (1×), dried over anhydrous sodium sulfate, and concentrated to a crude yellow oil. The crude oil was chromatographed on silica gel (20% ethyl acetate/hexanes) to give 3-{4-[2-(tert-butoxycarbonyl-heptyl-amino)-ethyl]-phenyl}-2-ethoxy-acrylic acid ethyl ester as a clear oil (700 mg, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699904B2
Source datasetuspto-grants-2004_03
ORD IDord-83ad992653574de698a11b0c55e23db4
Source noteuspto-grants-2004_03