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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245343Generated: October 30, 2026

Valeryl chloride → 2-(2-Pentanoyloxy-5-nitrophenyl)-1-(4-methoxyphenyl)-ethanone

https://huagongshe.com/reaction/245343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantValeryl chlorideHCID 61186—
Reactant2-(2-Hydroxy-5-nitrophenyl)-1-(4-methoxyphenyl)-ethanone potassium saltHCID 66687980—
SolventAcetoneHCID 180—
Product2-(2-Pentanoyloxy-5-nitrophenyl)-1-(4-methoxyphenyl)-ethanoneHCID 6668880198%

Reaction Steps

4.23 g (35.0 mmol) of valeroyl chloride (compound of the formula VI) were added with cooling at −10° C. to 20° C. to a stirred suspension of 11.3 g (34.7 mmol) of 2-(2-hydroxy-5-nitrophenyl)-1-(4-methoxyphenyl)-ethanone potassium salt (example 1) in 50 ml of dry acetone. After 30 minutes the reaction was complete, as monitored by LC-MS, and the mixture was filtered through a layer of Celite to remove the precipitated potassium chloride. The solution was evaporated to dryness to give 9.23 g (98%) of a yellow oil which slowly crystallized while standing at room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658808B2
Source datasetuspto-grants-2014_02
ORD IDord-835ecdb5ca6140f49b0b9dc67f9d4e95
Source noteuspto-grants-2014_02