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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259177Generated: October 30, 2026

Oxyphenbutazone → HCID 20391701, compound

https://huagongshe.com/reaction/259177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxyphenbutazoneHCID 4641—
ReactantAcetyl chlorideHCID 6367—
SolventAcetic AcidHCID 176—
ProductHCID 20391701HCID 20391701—

Reaction Steps

First, 1-Phenyl-2-(4'-acetyloxyphenyl)-3,5-pyrazolidinedione was prepared as follows. Oxyphenbutazone (1.00 g, 3.1 mmole) was suspended in 4 ml of glacial acetic acid and allowed to react with 2 ml of acetyl chloride at room temperature overnight. The solution was concentrated in vacuo at 86° C. to give a white residue (mp 126°-130° C.). The residue was crystallized from chloroformheptane (6:50) with cooling to give 0.81 g (mp 132°-134° C., 71% yield, lit., R. Pfester and F. Hafliger, Helvetica Chemica Acta, 40, 395 (1957) mp 135°-137° C. from methanol) of 1-phenyl-2-(4'acetyloxyphenyl)-3,5-pyrazolidinedione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04036845
Source datasetuspto-grants-1977_07
ORD IDord-34696864707b49bcbef2c1ac9b75d5e7
Source noteuspto-grants-1977_07