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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810607Generated: October 29, 2026

Acetonitrile → HCID 67045661, compound

https://huagongshe.com/reaction/1810607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantHexylamineHCID 8102—
ReactantHCID 10934655HCID 10934655—
ProductHCID 67045661HCID 67045661—

Reaction Conditions

Temperature70 °C

Reaction Steps

10 g (36 mmol) 4-(3-chloropropoxy)benzophenone was dissolved in 100 mL acetonitrile. 36.4 g (0.36 mol) n.-hexyl amine was added and the mixture was heated to 70° C. for 20 hours. The solvent was evaporated under reduced pressure. The oily residue was treated with 500 mL water. The mixture was acidified to pH=1 and stirred for 16 hours at room temperature. The precipitated compounds were isolated by filtration and washed with 200 mL 1 N HCl. The precipitate was treated with 200 mL 1 N NaOH. The mixture was extracted with 200 mL methylene chloride. The organic fraction was dried over MgSO4 and the solvent was evaporated under reduced pressure. The crude 4-[(3-hexylamino)propoxy]benzophenone was purified by preparative column chromatography on a Prochrom LC80 column, using Kromasil Si 60A 10 mm as silica and a gradient elution from methylene chloride to methylene chloride/methanol 68/32 at a flow rate of 150 mL per minute. 3.9 g of 4-[(3-hexylamino)propoxy]benzophenone was isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362101B2
Source datasetuspto-grants-2013_01
ORD IDord-d98c0524b20543d098969eb30d674c99
Source noteuspto-grants-2013_01