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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37457Generated: October 30, 2026

p-Anisoyl chloride → HCID 15288968, compound

https://huagongshe.com/reaction/37457

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
ReactantHCID 15672703HCID 15672703—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15288968HCID 15288968—

Reaction Steps

5.0 g (0.03 mol) of 5-(trifluoromethyl)-5-methylpyrrolidin-2-one in 10 ml of dioxane are stirred with 3.3 g of triethylamine and 6.8 g (0.04 mol) of anisoyl chloride for 16 h at 110°-120° C. The solid which precipitates is filtered off with suction and the salt is washed with a little dioxane. The dioxane solution is stirred into 50 ml of water and the organic phase is separated off with the addition of a little methylene chloride. After stripping off the solvent, the residue is a brownish solid which is recrystallized from ligroin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420293
Source datasetuspto-grants-1995_05
ORD IDord-dfff1a4aacc547a5862497ce58d60b50
Source noteuspto-grants-1995_05