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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329038Generated: October 25, 2026

Sodium Iodide → 2-Butanol, 3-((1-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)-4-piperidinyl)oxy)-

https://huagongshe.com/reaction/329038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
Reactant10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
Reactant1,2-Dimethyl-2-(4-piperidyloxy)-ethanolHCID 21440907—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-Butanol, 3-((1-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)-4-piperidinyl)oxy)-HCID 21809348%

Reaction Steps

22.5 g (0.15 mole) of sodium iodide were added to a solution of 51.5 g (0.15 mole) of 10-(3-chloropropyl)-2-trifluoromethyl-phenothiazine in 400 ml of methyl ethyl ketone followed by the addition of 15.2 g (0.15 mole) of triethylamine and then 26 g (0.15 mole) of 1,2-dimethyl-2-(4-piperidyloxy)-ethanol. The mixture was then refluxed for 20 hours and after cooling, the precipitate formed was removed by vacuum filtration. The filtrate was evaporated to dryness and the oil residue was chromatographed over 1 kg of neutral alumina. Elution with ethyl acetate gave 34.5 g (48% yield) of 2-trifluoromethyl-10-[3-(4-[1,2-dimethyl-2-hydroxyethoxy]-piperidino)-propyl]-phenothiazine in the form of a clear amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04018922
Source datasetuspto-grants-1977_04
ORD IDord-e8008bdff8df4e0796e205ef0c9844a3
Source noteuspto-grants-1977_04