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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709011Generated: October 30, 2026

Methyl iodide → HCID 71523276, compound

https://huagongshe.com/reaction/709011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 86681543HCID 86681543—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
ProductHCID 71523276HCID 71523276—

Reaction Steps

To a solution of 1-(cyclohexyl(methyl)amino)propan-2-yl 2,4,6-trimethylbenzoate (0.30 g, 0.946 mmol) in DCE (5 mL), methyl iodide (0.12 mL, 1.892 mmol) was added. The resultant reaction mixture was stirred at rt for 16 hours. The reaction mixture was diluted with DCM and concentrated to dryness. The crude product was subjected to column chromatography to obtain N,N-dimethyl-N-[2-((2,4,6-trimethylbenzoyl)oxy)propyl]cyclohexanaminium iodide. Yield: 0.109 g (25%). 1H NMR (400 MHz, CDCl3) δ 6.86 (s, 2H), 5.70-5.67 (m, 1H), 4.52-4.48 (d, J=14 Hz, 1H), 3.83-3.77 (m, 1H), 3.70-3.64 (m, 1H), 3.34 (s, 3H), 3.28 (s, 3H), 2.29-2.01 (m, 10H), 2.01-1.98 (m, 1H), 1.84 (m, 1H), 1.64-1.62 (d, J=6 Hz, 4H), 1.47-1.38 (m, 4H), 1.13-1.08 (m, 2H). LCMS: m/z=332.2 [M+], RT=3.01 min (Column: Y, Program: P1). HPLC: 99.53% (200 nm), RT 4.11 min (Mobile phase: A: ACN, B: 0.05% TFA in water, Column: Zorbax® SBC18 (50*4.6 mm) 1.8μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180115B2
Source datasetuspto-grants-2015_11
ORD IDord-411133679d404c6bba0f38fd1315869c
Source noteuspto-grants-2015_11