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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307533Generated: November 1, 2026

Pyridine → HCID 69946252, compound

https://huagongshe.com/reaction/2307533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl chloroformateHCID 6586—
Reactant1,4-Dithiane-2,5-diolHCID 98330—
Reactant2-oxoethyl BenzoateHCID 10866664—
SolventDichloromethaneHCID 6344—
ProductHCID 69946252HCID 69946252—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 17.93 g (0.118 mmol) of mercaptoacetaldehyde dimer and 38.70 g (0.236 mmol) of benzoyloxyacetaldehyde in 57.3 mL (3 eq) of pyridine was heated until all the solid dissolved. After cooling, 300 mL of anhydrous methylene chloride were added and the mixture was cooled at 0° C. for ca. 30 minutes. To this solution at 0° C., was slowly added a solution of methylchloroformate (57.3 mL, 0.71 mmol) in 80 mL of methylene chloride. The mixture was stirred for 12 hrs and diluted with ca. 200 mL of methylene chloride and washed several times with brine to remove pyridinium salt and then the organic layer was washed with water. The organic layer was dries over magnesium sulphate at 0° C. and then filtered. Residual pyridine was removed in vacuo and the organic residue was purified by flash chromatography using hexanes:ethyl acetate (2:1) as eluent to yield a mixture of 2:1 trans:cis carbonates (56.3 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831174B2
Source datasetuspto-grants-2004_12
ORD IDord-f9168fa0dd664de3830adc6855fbdf86
Source noteuspto-grants-2004_12