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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765840Generated: October 30, 2026

Methyl iodide → HCID 57424256, compound

https://huagongshe.com/reaction/1765840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopropylamineHCID 69828—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 69073588HCID 69073588—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventSodium CarbonateHCID 10340—
ProductHCID 57424256HCID 5742425653%

Reaction Steps

A solution of {4-[8,8-dimethyl-5-oxo-4-(2-propoxy)-5,6,7,8-tetrahydro-naphthalen-2-ylethynyl]-phenyl}-acetic acid methyl ester (Intermediate 128, 0.07 g, 0.187 mmol) in dichloromethane (3 mL) and acetonitrile (1.5 mL) was treated with cyclopropyl amine (1 mL, 14.45 mmol). After 5 minutes, acetic acid (1 mL) was added followed by sodium cyanoborohydride (0.12 g, 1.91 mmol). The reaction mixture was stirred overnight at ambient temperature. It was then diluted with water and saturated aqueous sodium carbonate solution and extracted with dichloromethane (×2). The combined organic extract was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to an oil. The oil was dissolved in acetone (15 mL) and treated with potassium carbonate (0.2 g, 1.45 mmol)-followed by methyl iodide (1-mL, 15.8 mmol) and the resulting reaction mixture was stirred overnight at ambient temperature. The precipitated solids were filtered off, the filtrate was evaporated in vacuo to a residue. Flash column chromatography over silica gel (230–400 mesh) using 2.5–6% ethyl acetate in hexane as the eluent afforded the title compound (0.045 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226951B2
Source datasetuspto-grants-2007_06
ORD IDord-655e1b57e6464f4bbf7ae9fe4ce91da2
Source noteuspto-grants-2007_06