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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494436Generated: October 30, 2026

Acetyl chloride → HCID 14673827, compound

https://huagongshe.com/reaction/1494436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 19828167HCID 19828167—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14673827HCID 14673827—
ProductHCID 14673828HCID 14673828—

Reaction Steps

N-Hydroxy-N-(1-(4-(1-(4-fluorophenyl)ethoxy)-phenyl)ethyl]acetamide was prepared by the reaction of the hydroxylamine compound prepared in step (d) above with two equivalents of acetyl chloride in the presence of triethylamine in THF. The intermediate N,O-diacetyl compound was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, after which the solvent was evaporated. The residue was taken up in isopropyl alcohol and a solution of lithium hydroxide in water was added. The mixture was stirred until the reaction was complete, and then neutralized by the addition of 2N HCl. This mixture was extracted with ether, the ether solution dried over anhydrous magnesium sulfate, and evaporated to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026729
Source datasetuspto-grants-1991_06
ORD IDord-0b1e70dfe9124df895d08eb58cf10cc4
Source noteuspto-grants-1991_06