HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976796Generated: November 1, 2026
Benzyl chloroformate → HCID 178522340, compound
https://huagongshe.com/reaction/1976796
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Cytosine | HCID 178418229 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178522340 | HCID 178522340 | — |
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 4 N 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06228982B1 |
|---|
| Source dataset | uspto-grants-2001_05 |
|---|
| ORD ID | ord-1003c5ad1e7646ff8497af1cd200d164 |
|---|
| Source note | uspto-grants-2001_05 |
|---|