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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264247Generated: October 31, 2026

Methyl 4-iodobenzoate → Methyl 4-[3-[[(1,1-dimethylethoxy)carbonyl]amino]-1-propyn-1-yl]benzoate

https://huagongshe.com/reaction/1264247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-iodobenzoateHCID 69273—
Reactanttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventPiperidineHCID 8082—
ProductMethyl 4-[3-[[(1,1-dimethylethoxy)carbonyl]amino]-1-propyn-1-yl]benzoateHCID 1861767967%

Reaction Steps

Methyl-4-iodobenzoate (1.5 g, 5.7 mmol) and t-butyl prop-2-ynylcarbamate (0.89 g, 5.7 mmol, reference example 82) are dissolved in piperidine (12 mL) and this solution purged with nitrogen. Copper(I) iodide (22 mg, 0.11 mmol) and dichlorobis(triphenylphosphine) palladium (40 mg, 0.057 mmol) is added and the mixture is stirred at R.T. After 2 hours, the solvent is removed in vacuo and the residue added to CH2Cl2 and washed with 1N HCl, water and brine, then dried over magnesium sulfate. The solvent is removed in vacuo and the residue purified by flash chromatography, eluting with 20% ethyl acetate/hexane to provide the title compound as a white solid (1.1 g, 67% yield): 1H NMR (300 MHz, CDCl3) d 7.98 (d, 2H), 7.48 (d, 2H), 4.79 (bs, 1H), 4.17 (d, 2H), 3.91 (s, 3H), 1.48 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541505B1
Source datasetuspto-grants-2003_04
ORD IDord-e82b8e49f2804b8dbc00dedb8a5ffbbf
Source noteuspto-grants-2003_04