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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051863Generated: November 1, 2026

2-Chloroethyl chloroformate → HCID 68002661, compound

https://huagongshe.com/reaction/1051863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl chloroformateHCID 12305—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-3-methoxyanilineHCID 7018254—
SolventAcetonitrileHCID 6342—
ProductHCID 68002661HCID 6800266117.1%

Reaction Steps

To a stirred solution of 4-Bromo-3-methoxy-aniline (10.0 g) in acetonitrile (176 mL) was added Hünig Base (25 mL) and 2-chloroethyl chloroformate (10.6 g). The mixture was stirred at room temperature for 0.5 h. The solvent was removed in vacuum. The residue was dissolved in tetrahydrofurane (250 mL), and potassium tert-butoxide (16.2 g) was added. The mixture was stirred at room temperature for 2 h. The solvent was removed in vacuum. The residue was dissolved in ethyl acetate and the mixture was washed with water and with saturated sodium chloride solution, dried (sodium sulfate) and the solvent was removed in vacuum. Silica gel chromatography gave a compound that was crystallized from ethanol. Yield: 7.7 g of the title compound. The mother liquor was concentrated in vacuum and aminophase-silica-gel chromatography gave a solid that was recrystallized from ethanol to give further 2.3 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388177B2
Source datasetuspto-grants-2016_07
ORD IDord-21cd23f96f004b469e229def0205af21
Source noteuspto-grants-2016_07