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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265481Generated: October 28, 2026

Water → 1-[4-(3-Chloropropoxy)-3-dimethylaminophenyl]ethanone

https://huagongshe.com/reaction/265481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
ReactantHCID 12225608HCID 12225608—
SolventDimethylformamideHCID 6228—
Product1-[4-(3-Chloropropoxy)-3-dimethylaminophenyl]ethanoneHCID 10106428179%

Reaction Conditions

Temperature3 °C

Reaction Steps

To a suspension of sodium hydride (2.3 g, 48.5 mmol of 50% oil dispersion) with dimethylformamide (75 ml), and cooled to 3° C. in an ice-salt bath and under a stream of nitrogen was added, dropwise, 1-(4-hydroxy-3-dimethylaminophenyl)ethanone (8.7 g, 48.5 mmol) dissolved in dimethylformamide (150 ml) so that the temperature did not go over 7° C. After the addition was over, the bath was removed and the reaction was stirred at ambient temperature for 45 minutes. The ice bath was reapplied and a solution of 1-bromo-3-chloropropane (8.4 g, 53.4 mmol) in dimethylformamide (25 ml) was added dropwise. After the addition was complete, the reaction was stirred for 18 hours at ambient temperature under nitrogen. The reaction was chilled to 7° C. in an ice bath and water (200 ml) was carefully added. After stirring for 5 minutes, the aqueous mixture was extracted with ethyl acetate (5×200 ml). The ethyl acetate extract was washed with water (2×50 ml), dried with MgSO4, and concentrated to yield 22.2 g of a black oily liquid. The compound was purified by prep HPLC, and combination of appropriate fractions gave 5.0 g of brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648363
Source datasetuspto-grants-1997_07
ORD IDord-e739e2b1050c4fb9814451eb6179584e
Source noteuspto-grants-1997_07