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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601146Generated: October 31, 2026

Methyl chloroformate → HCID 21831182, compound

https://huagongshe.com/reaction/1601146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21831175HCID 21831175—
SolventDichloromethaneHCID 6344—
ProductHCID 21831182HCID 21831182—

Reaction Conditions

Temperature25 °C

Reaction Steps

2.1 g (22 mmol) of methyl chloroformate were added dropwise at -10° C. to a mixture of 4.3 g (mmol) of N-[2-(2-methylphenoxymethyl)pyridin-3-yl]hydroxylamine (Example 3.e), 3.3 g (39 mmol) of NaHCO3 (solid) and 50 ml of methylene chloride. After the reaction mixture had been stirred for 4 hours at room temperature (approximately 25° C.), it was washed with water, dried and freed from solvent under reduced pressure. The residue was purified by column chromatography (cyclohexane/ethyl acetate). This gave 0.6 g (10%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977146
Source datasetuspto-grants-1999_11
ORD IDord-9d72895ddf484c85a0c550adabd33d4c
Source noteuspto-grants-1999_11