Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033288Generated: November 1, 2026

Benzoyl chloride → HCID 22851614, compound

https://huagongshe.com/reaction/1033288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 12081666HCID 12081666—
SolventPyridineHCID 1049—
ProductHCID 22851614HCID 2285161492%

Reaction Steps

After 1 g (2.7 mmols) of 5'-O-acetyl-3'-deoxy-3'-bromoadenosine was added to 10 ml of pyridine, 418 mg (1.1 eq.) of benzoyl chloride was added to the mixture. The mixture was stirred at room temperature for 2 hours and pyridine was distilled off under reduced pressure. The residue was added to 30 ml of water followed by extraction twice with 30 ml of chloroform. After the organic solvent was washed with water and then dried over magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography to give 1.18 g (yield, 92%) of 2'-O-benzoyl-5'-O-acetyl-3'-deoxy-3'-bromoadenosine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310895
Source datasetuspto-grants-1994_05
ORD IDord-83bd38bee1204dfa9a4611cb02104039
Source noteuspto-grants-1994_05