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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817676Generated: October 30, 2026

Ammonium Chloride → HCID 57801035, compound

https://huagongshe.com/reaction/1817676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantN-Methoxy-N-methyl-4-phenylbenzamideHCID 10060247—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57801035HCID 5780103570%

Reaction Steps

5-Bromo-1-pentene (1.5 g) was gently heated with magnesium turnings (1 g) in anhydrous tetrahydrofuran (15 ml) until reaction started. The mixture was left to reflux without further heating to give the Grignard reagent, then allowed to cool to room temperature. Biphenyl-4-carboxylic acid methoxy-methyl amide (4 g) was dissolved in anhydrous tetrahydrofuran (20 ml) and chilled in an ice bath. The Grignard reagent was added dropwise with vigorous stirring. Following addition, the mixture was allowed to warm to room temperature and stirring continued for 2 hours. Saturated NH4Cl solution (50 ml) was added and the mixture extracted with petrol. Drying with Na2SO4 followed by evaporation gave an oil. Column chromatography (petrol:ethyl acetate 5:1) gave the title compound as a white solid (70%). δC (CDCl3, 62.9 MHz): 23.4, 33.3, 37.8, 115.4, 127.3, 127.3, 128.2, 128.7, 129.0, 135.8, 138.1, 139.9, 145.6 and 199.9. δH (CDCl3, 250 MHz): 1.88 (2H, quintet, J 7.32), 2.17 (2H, quintet, J 7.32), 3.00 (2H, t, J 7.32), 5.03 (2H, m), 5.84 (1H, m), 7.62 (2H, d, J 7.9), 7.47 (3H, m), 7.67 (2H, d, J 7.9) and 8.03 (2H, d, J 7.9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598289B2
Source datasetuspto-grants-2009_10
ORD IDord-e7c8389f92f5441bb0f5479a56f1dd32
Source noteuspto-grants-2009_10