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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744876Generated: November 3, 2026

Anisole → HCID 19422436, compound

https://huagongshe.com/reaction/744876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantHCID 19422423HCID 19422423—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 19422436HCID 1942243698.9%

Reaction Steps

To 3.74 g of 1-(p-methoxybenzyloxycarbonyl)-4-(2-(p-nitrobenzyloxycarbonyl)aminoacetyl)piperazine were added 4.17 ml of anisole and, with cooling on an ice bath, 20 ml of trifluoroacetic acid, followed by 1 hour of reaction at room temperature. After removing trifluoroacetic acid by evaporation under a reduced pressure, the residue was adjusted to basic with a sodium hydroxide aqueous solution and extracted with chloroform, and an organic layer was washed with water and dried over sodium sulfate, followed by removal of the solvent under a reduced pressure and subsequent addition of n-hexane to a residue to collect a solid material by filtration, thereby obtaining 2.45 g of 1-(2-(p-nitrobenzyloxycarbonyl)aminoacetyl)piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559224
Source datasetuspto-grants-1996_09
ORD IDord-3be2f55d706545cfaafe345b2f2f729c
Source noteuspto-grants-1996_09