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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667105Generated: November 2, 2026

Acetic Acid → HCID 67445097, compound

https://huagongshe.com/reaction/1667105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3'-(Trifluoromethyl)acetophenoneHCID 67682—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventEthanolHCID 702—
ProductHCID 67445097HCID 67445097—

Reaction Conditions

Temperature75 °C

Reaction Steps

A suspension of 1-(3-(trifluoromethyl)phenyl)ethanone (0.100 g, 0.532 mmol), tert-butyl piperazine-1-carboxylate (0.148 g, 0.797 mmol), acetic acid (0.046 mL, 0.797 mmol) and sodium cyanoborohydride (0.050 g, 0.797 mmol) in ethanol (0.5 mL) was heated under nitrogen at 75° C. After stirring overnight the reaction was concentrated, saturated sodium bicarbonate (0.7 mL) was added, and the product was extracted into ethyl acetate (2×0.7 mL). The combined organic layers were concentrated, dissolved in a minimal amount of dichloromethane, loaded directly onto a SF15-12 silica gel column (Analogix®, Burlington, Wis.), and the title compound was eluted using a gradient of 2% to 20% ethyl acetate/hexanes over 20 minutes (flow=30 mL/minute).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044069B2
Source datasetuspto-grants-2011_10
ORD IDord-55d43212932b45bca2f1bc063c5f5a5a
Source noteuspto-grants-2011_10