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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210722Generated: November 1, 2026

Methanol → HCID 21689652, compound

https://huagongshe.com/reaction/2210722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantEpichlorohydrinHCID 7835—
Reactant1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
SolventEthanolHCID 702—
ProductHCID 21689652HCID 21689652100,783.602%

Reaction Steps

To a mixture of epichiorohydrin (3.5 mL, 0.05 mmol) in ethanol (12 mL) at 0° C. (ice bath) and anhydrous NaH-CO3 (4.2 g, 0.05 mmol), [bis(4-fluorophenyl)methyl]piperazine (14.4 g, 0.05 mmol) in ethanol (200 mL) was added dropwise over 45 min under N2. The ice bath was removed and the mixture was allowed to come to room temperature. After 18 h the NaHCO3 was removed by filtration via a sintered glass funnel and the ethanol in the filtrate was removed in vacuo to give the crude product (21.3 g). Silica gel flash chromatography using 2.0% MeOH:CH2Cl2 gave pure product (10.05 g, 52.9%) as an amber oil. DCI/MS (M+1) 381.400 MHz 1H NMR (CDCl3)δ: 7.3 (m, 4H), 6.95 (m, 4H), 4.2 (s, 1H), 3.95 (m, 1H), 3.55 (m, 2H), 2.7 (m, 2H), 2.5 (m, 4H), 2.4 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE035072
Source datasetuspto-grants-1995_10
ORD IDord-404a6b5af046431b8364e530edd8b17d
Source noteuspto-grants-1995_10