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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709017Generated: October 29, 2026

Methyl iodide → HCID 71522298, compound

https://huagongshe.com/reaction/709017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 86681546HCID 86681546—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 71522298HCID 71522298—

Reaction Steps

To a solution of 1-(cyclohexyl(methyl)amino)propan-2-yl 4-isopropylbenzoate (0.5 g, 1.57 mmol) in DCE (5 mL, methyl iodide (0.2 mL, 3.15 mmol) was added. The resultant reaction mixture was stirred at rt for 16 hours. The solvent was evaporated, and the crude product was purified by column chromatography. The product isolated was re-crystallized from methanol/ether. Yield: 134.9 mg (18.65%). 1H NMR (400 MHz, DMSO-d6) δ 7.94-7.92 (d, J=8 Hz, 2H), 7.43-7.41 (d, J=8 Hz, 2H), 5.54-5.50 (m, 1H), 3.95-3.89 (m, 1H), 3.61-3.58 (d, J=14 Hz, 1H), 3.40-3.34 (m, 1H), 3.03-2.95 (m, 7H), 2.22-2.20 (d, J=11 Hz, 1H), 2.10-2.07 (d, J=11 Hz, 1H), 1.86-1.83 (m, 2H), 1.57-1.43 (m, 3H), 1.36-1.35 (d, J=6 Hz, 3H), 1.16-1.11 (m, 9H). LCMS: m/z=331.8 [M+], RT=3.08 min (Column: Y, Program: P1). UPLC: 99.65% (200 nm), RT 3.09 min (Mobile phase: A. ACN, B. 0.05% HCOOH in water, Column: Gemini® NX C18 (50*4.6 mm) 3μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180115B2
Source datasetuspto-grants-2015_11
ORD IDord-07315f7b60304ec2b41b7d119418e027
Source noteuspto-grants-2015_11