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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810605Generated: November 3, 2026

Sodium Iodide → HCID 58194624, compound

https://huagongshe.com/reaction/1810605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMethylamineHCID 6329—
ReactantHCID 58184920HCID 58184920—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 58194624HCID 58194624—

Reaction Conditions

Temperature60 °C

Reaction Steps

26 g (85 mmol) 2-(3-chloropropoxy)-9H-thioxanthen-9-one is suspended in 140 mL acetonitrile. 66 g (73.2 mL, 0.85 mol) of a 40% solution of methyl amine in water was added and the mixture was heated to 60° C. After four hours, 1.3 g (8.5 mmol) sodium iodide and 20 mL of a 40% solution of methyl amine in water were added and the reaction was allowed to continue for 16 hours at 60° C. The precipitated compounds were isolated by filtration and washed three times with 100 mL acetonitrile. The pooled acetonitrile fractions were evaporated under reduced pressure. The crude 2-(3-methylaminopropoxy)thioxanthen-9-one was crystallized from 200 mL hexane, isolated by filtration and dried. 19 g of 2-(3-methylaminopropoxy)thioxanthen-9-one was isolated. 2-(3-methylaminopropoxy)thioxanthen-9-one was further purified by preparative column chromatography on a Prochrom LC80 column, using Kromasil C18 100A 10 mm as silica and methanol/1M ammonium acetate 68/32 as eluent at a flow rate of 150 mL per minute.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362101B2
Source datasetuspto-grants-2013_01
ORD IDord-9fcc138faf624b88aaf6c6d97d0c65fe
Source noteuspto-grants-2013_01