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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21908Generated: October 25, 2026

Ethyl cyanoacetate → Methyl 4-(4-cyano-4-ethoxycarbonylbutyl)benzoate

https://huagongshe.com/reaction/21908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantMethyl 4-(3-hydroxypropyl)benzoateHCID 14425137—
ReactantMethyl-(4-cyano-4-ethoxycarbonylbutyl)benzoateHCID 86748740—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(4-cyano-4-ethoxycarbonylbutyl)benzoateHCID 1993089140%

Reaction Steps

Preparation of methyl-(4-cyano-4-ethoxycarbonylbutyl)benzoate ##STR21## To a 250 mL flame dried round bottom flask were charged 10.0 g (51.5 mmol) of methyl 4-(-hydroxypropyl)benzoate and 5.48 mL (51.5 mmol) of ethyl cyanoacetate dissolved in 40 mL of anhydrous tetrahydrofuran (THF). To this solution was then added dropwise to a solution of 20.2 g (77 mmol) of triphenylphosphine and 12.1 mL (77 mmol) of diethyl azodicarboxylate dissolved in 60 mL of anhydrous THF. After the addition, the reaction was stirred at ambient temperature for 1.5 hours. The volatiles were removed in vacuo and the crude oil was dissolved in 300 mL of EtOAc, washed with brine, dried over Na2SO4, and removed in vacuo. This crude oil was then purified on silica gel using a Waters Prep LC 2000 eluting with a gradient of 1:1 MeCl2 /Hex to 100% MeCl2 to give 6.0 g (40%) of methyl 4-(4-cyano-4-ethoxycarbonylbutyl)benzoate as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426110
Source datasetuspto-grants-1995_06
ORD IDord-79485092b152460b8534aa79e42ca71f
Source noteuspto-grants-1995_06