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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762874Generated: October 30, 2026

Sodium Chloride → HCID 20039945, compound

https://huagongshe.com/reaction/1762874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant4-BenzyloxyanilineHCID 22860—
ReactantCesium fluorideHCID 25953—
ReactantHeptanenitrile, 7-bromo-HCID 88737—
SolventDimethylformamideHCID 6228—
ProductHCID 20039945HCID 2003994585%

Reaction Conditions

Temperature100 °C

Reaction Steps

A 20 g portion of 4-benzyloxyaniline hydrochloride was dissolved in chloroform-methanol and made basic with a solution of 70 mL of 1.25N sodium hydroxide and 70 mL of water. The layers were separated, the aqueous phase extracted with chloroform, the chloroform extracts washed with saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was evaporated to yield 17 g of 4-benzyloxyaniline. A solution of 2 g (0.01 mol) of 4-benzyloxyaniline, 2.26 ml (0.015 mol) of 7-bromoheptanenitrile and 7.6 g (0.05 mol) of cesium fluoride in 20 mL of DMF was stirred and heated at 100° C. for two hours. The reaction was cooled and poured into saturated sodium chloride solution and extracted with ether. The ether extracts were washed three times with saturated sodium chloride solution, dried over magnesium sulfate and concentrated to 2.9 g of oil. The oil was chromatographed on 100 g of silica gel using a gradient from 10-30% ethyl acetate in hexane. There was obtained 2.55 g (85%) of 7-[(4-benzyloxyphenyl)amino]heptanenitrile. The benzyloxy compound was treated with eight parts of 48% HBr at room temperature for 5 hours to yield impure 7-[(4-hydroxyphenyl)amino]heptanenitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835180
Source datasetuspto-grants-1989_05
ORD IDord-1da6874857a44c20bc9093a1e8f78fad
Source noteuspto-grants-1989_05