Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544728Generated: October 29, 2026

Acetic Anhydride → HCID 20458181, compound

https://huagongshe.com/reaction/544728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 20458191HCID 20458191—
CatalystPyridineHCID 1049—
ProductHCID 20458181HCID 20458181—

Reaction Steps

A few drops of pyridine are added to a solution of 26.7 g (0.12 mole) of 3-[2-hydroxy-5-methyl-4-(pyrrol-1-yl)-phenyl]-1-butene in 370 ml of acetic anhydride and the mixture is stirred at room temperature for 2 hours. The reaction mixture is poured onto ice and extracted three times with methylene chloride. The methylene chloride phases are washed with dilute sodium bicarbonate solution, then with water, until neutral, are combined, dried over sodium sulphate and concentrated in a vacuum rotary evaporator. Filtration over a little silica gel with methylene chloride yields 3-[2-acetoxy-5-methyl-4-(pyrrol-1-yl)-phenyl]-1-butene, Rf (toluene/ethyl acetate=10:1): 0.55.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04451462
Source datasetuspto-grants-1984_05
ORD IDord-80e73ddec4064a3e926abda6fab3799d
Source noteuspto-grants-1984_05