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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735952Generated: October 30, 2026

Pyridine → HCID 178522340, compound

https://huagongshe.com/reaction/1735952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzyl chloroformateHCID 10387—
ReactantHCID 19076265HCID 19076265—
ProductHCID 178522340HCID 178522340—

Reaction Conditions

Temperature0 °C

Reaction Steps

Over a period of about 1 h, benzyloxycarbonyl chloride (52 ml; 0.36 mol) was added dropwise to a suspension of cytosine (8, 20.0 g; 0.18 mol) in dry pyridine (1000 ml) at 0° C. under nitrogen in oven-dried equipment. The solution then was stirred overnight, after which the pyridine suspension was evaporated to dryness, in vacuo. Water (200 ml) and 4N hydrochloric acid were added to reach pH~1. The resulting white precipitate was filtered off, washed with water and partially dried by air suction. The still-wet precipitate was boiled with absolute ethanol (500 ml) for 10 min, cooled to 0° C., filtered, washed thoroughly with ether, and dried, in vacuo. Yield 24.7 g (54%). M.p.>250° C. Anal. for C12H11N3O3. Found (calc.); C: 58.59(58.77); H: 4.55(4.52); N: 17.17(17.13). No NMR spectra were recorded since it was not possible to get the product dissolved.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05539082
Source datasetuspto-grants-1996_07
ORD IDord-09ecc43c3f1649fb90123f272f8df593
Source noteuspto-grants-1996_07