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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839610Generated: October 30, 2026

Benzyl chloroformate → HCID 20323724, compound

https://huagongshe.com/reaction/839610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantHexamethylphosphoramideHCID 12679—
ReactantSodium hydrideHCID 24758—
ReactantN-(2,2-Diethoxyethyl)pyridin-4-amineHCID 71373211—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 20323724HCID 2032372411.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 4-pyridylaminoacetaldehyde diethyl acetal (7.0 g.) in a mixture of dried dimethylformamide (20 ml.) and dried hexamethylphosphoric triamide (7.5 ml.) was dropwise added over 5 minutes under ice-cooling and stirring to a suspension of 65.5% sodium hydride (2.0 g.) in dried dimethylformamide (3 ml.). The mixture was stirred for 10 minutes at ambient temperature, for 30 minutes at 60° C and for 15 minutes under ice-cooling. A solution of benzyl chloroformate (9.0 g.) in dried dimethylformamide (2 ml.) was dropwise added thereto under stirring and ice-cooling. The resulting mixture was stirred for 20 minutes under ice-cooling and for 15 minutes at ambient temperature. After water was dropwise added to the reaction mixture, the mixture was extracted 3 times with ethyl acetate. The extract was in turn washed twice with water and once with a saturated sodium chloride aqueous solution and dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the residual oil was purified by column chromatography on silica gel (60 g.) using a mixture of benzene and ethyl acetate (7 : 3) as developing solvent to give oil of N-benzyloxycarbonyl-N-(4-pyridyl)aminoacetaldehyde diethyl acetal (1.3 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04096263
Source datasetuspto-grants-1978_06
ORD IDord-cb2217c019544f92ac214b437826121d
Source noteuspto-grants-1978_06