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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456955Generated: October 25, 2026

Dichloromethane → Ammonia dichloromethane

https://huagongshe.com/reaction/456955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-ChloroanilineHCID 7812—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-[3-(1-Piperidinyl)propoxy]benzaldehydeHCID 13795259—
SolventAcetic AcidHCID 176—
Product(4-Chloro-phenyl)-[2-(3-piperidin-1-yl-propoxy)-benzyl]-amineHCID 17962633—
ProductAmmonia dichloromethaneHCID 227314291%

Reaction Steps

A solution of 2-(3-piperidin-1-yl-propoxy)-benzaldehyde (266 mg), 4-chloroaniline (146 mg), and acetic acid (0.07 mL) in DCM (5 mL) was treated with sodium triacetoxyborohydride (400 mg). After 16 h, the resulting mixture was treated with 10% sodium hydroxide (6 mL) and extracted with DCM (3×10 mL). The combined organic phases were dried (sodium sulfate) and evaporated. Chromatography of the residue (1–5% 2 M methanolic ammonia/DCM) gave the title compound as a colorless oil (246 mg). 1H NMR (400 MHz, CDCl3): 7.28–7.20 (m, 2H), 7.09 (d, J=8.9 Hz, 2H), 6.89 (m, 2H), 6.55 (d, J=8.9 Hz, 2H), 4.30 (d, J=5.6, 2H), 4.18 (m, 1H), 4.05 (t, J=6.3 Hz, 2H), 2.47 (m, 2H), 2.37 (br, 4H), 1.96 (m, 2H), 1.62–1.56 (m, 4H), 1.49–1.42 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186732B2
Source datasetuspto-grants-2007_03
ORD IDord-68e86e996bd247a8b340c25adcb0f288
Source noteuspto-grants-2007_03