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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481523Generated: November 1, 2026

Methyl chloroformate → HCID 67410811, compound

https://huagongshe.com/reaction/1481523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 22990479HCID 22990479—
SolventAcetonitrileHCID 6342—
ProductHCID 67410811HCID 67410811—

Reaction Steps

To a mixture of 4-tert-butyl-1-methyl-1H-imidazole (800 mg, 5.79 mmol, prepared as described in the previous step) and triethylamine (2.00 mL, 14.4 mmol) in acetonitrile (10 mL) at −30° C. was added methyl chloroformate (0.890 mL, 11.6 mmol) slowly under Ar. The resulting mixture was warmed to room temperature and continued to stir for 16 h. The resulting mixture was then treated with EtOAc (50 mL) and washed with H2O (2×20 mL), brine (20 mL) and then dried with Na2SO4. The solvent was evaporated in vacuo and the residue was purified by flash chromatography on silica gel (0:100-10:90 MeOH/DCM) to yield 4-tert-butyl-1-methyl-1H-imidazole-2-carboxylic acid methyl ester as a colorless oil. 1H-NMR (400 MHz, CDCl3) δ: 6.78 (s, 1H), 3.95 (s, 3H), 3.92 (s, 3H), 1.30 (s, 9H). Mass Spectrum (LCMS, ESI pos.) Calculated For C10H16N2O2: 197.1 (M+H). Measured: 197.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409915B2
Source datasetuspto-grants-2016_08
ORD IDord-ae2cb31640254a4498cff011e7557dd5
Source noteuspto-grants-2016_08