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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278188Generated: November 1, 2026

1,2-Dichloroethane → HCID 89682752, compound

https://huagongshe.com/reaction/2278188

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Fluoro-4-morpholin-4-ylbenzaldehydeHCID 7148609—
Reactanttert-Butyl (2S)-2-methylpiperazine-1-carboxylateHCID 10081508—
SolventWaterHCID 962—
ProductHCID 89682752HCID 8968275293.1%

Reaction Steps

A 100 mL round-bottom flask was charged with 2-fluoro-4-(morpholin-4-yl)benzaldehyde (0.800 g, 3.82 mmol, 1.00 equiv), tert-butyl (2S)-2-methylpiperazine-1-carboxylate (0.840 g, 4.20 mmol, 1.10 equiv), 1,2-dichloroethane (20 mL). The mixture was stirred for 30 min at room temperature. Sodium triacetoxyborohydride (2.40 g, 11.3 mmol, 3.00 equiv) was added. The resulting solution was stirred overnight at room temperature, diluted with H2O (10 mL), extracted with dichloromethane (3×10 mL). The organic layers were combined and washed with brine (50 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was chromatographed on a silica gel column with ethyl acetate/petroleum ether (25/75) to provide 1.40 g (93% yield) of tert-butyl (2S)-4-[[2-fluoro-4-(morpholin-4-yl)phenyl]methyl]-2-methylpiperazine-1-carboxylate as a white solid. LCMS (ESI, m/z): 394 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133148B2
Source datasetuspto-grants-2015_09
ORD IDord-49ec8b1506344a5abd9904977f375fa5
Source noteuspto-grants-2015_09