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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530211Generated: November 2, 2026

Acetonitrile → (S)-1-(3-(ethyl(methyl)carbamoyloxy)phenyl)-N,N-dimethyl-N-((S)-1-phenylethyl)ethanaminium iodide

https://huagongshe.com/reaction/530211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium HydroxideHCID 14797—
ReactantN-Ethyl-N-methylcarbamoyl chlorideHCID 11240471—
ReactantHCID 86712421HCID 86712421—
SolventEthylene GlycolHCID 174—
Product(S)-1-(3-(ethyl(methyl)carbamoyloxy)phenyl)-N,N-dimethyl-N-((S)-1-phenylethyl)ethanaminium iodideHCID 86712425—

Reaction Conditions

Temperature60 °C

Reaction Steps

Mix 7.9 g (0.02 mol) of (S)-1-(3-hydroxyphenyl)-N,N-dimethyl-N—((S)-1-phenylethyl)ethanaminium iodide (formula VIII) with 180 ml of acetonitrile, 1.7 g (0.03 mol) of potassium hydroxide, 3.6 (0.03 mol) ethyl(methyl)carbamic chloride and 0.1 g of macrogol 400 at room temperature, heat it to 60° C. and react it for 12 hours. After it is cooled to room temperature, filter it and reduce the pressure to recover the solvent and receive 10.2 g of red-brown liquid to be directly used in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353049B2
Source datasetuspto-grants-2016_05
ORD IDord-d4ff81d75b4f457b999f564a9d9c2c6c
Source noteuspto-grants-2016_05