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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103728Generated: October 30, 2026

N-(4-cyanophenyl)acetamide → HCID 69058617, compound

https://huagongshe.com/reaction/2103728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-cyanophenyl)acetamideHCID 37256—
Reactant1-Chloro-4-iodobutaneHCID 82527—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 69058617HCID 69058617—

Reaction Steps

9 g (54.1 mmol) of N-(4-cyanophenyl)acetamide are dissolved in 100 ml of THF. The mixture is cooled to 0° C. before the dropwise addition of 51 ml of a 1.6 N solution in hexane of nBuLi (1.5 eq.). The solution is left for one hour to return to ambient temperature and is then cooled to 0° C. before the dropwise addition of 9.9 ml of 1-chloro-4-iodobutane (81 mmol). The reaction mixture is stirred at ambient temperature for 18 h and then hydrolysed with a saturated aqueous solution of ammonium chloride (100 ml) and extracted with ethyl acetate. The organic phases are combined, dried over magnesium sulphate and concentrated. Purification by chromatography on silica (eluant: petroleum ether/ethyl acetate: 1/1) yields a yellow oil containing the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576120B2
Source datasetuspto-grants-2009_08
ORD IDord-a18af5e5e0c34bc6afafaff429a11712
Source noteuspto-grants-2009_08