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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456948Generated: October 27, 2026

1,2-Dichloroethane → Ammonia dichloromethane

https://huagongshe.com/reaction/456948

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantSodium HydroxideHCID 14798—
Reactant4-(3-Piperidin-1-ylpropoxy)benzaldehydeHCID 2766324—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
ProductDimethyl-[4-(3-piperidin-1-yl-propoxy)-benzyl]-amineHCID 9835304—
ProductAmmonia dichloromethaneHCID 227314293%

Reaction Steps

A solution of the product of Example 9 (175 mg), dimethylamine hydrochloride (64 mg), and acetic acid (0.05 mL) in DCE (3 mL) was treated with sodium triacetoxyborohydride (210 mg). After 16 h, the resulting mixture was treated with 10% sodium hydroxide (1 mL) and extracted with DCM (3×3 mL). The combined organic phases were dried (magnesium sulfate) and evaporated. Chromatography of the residue (3% 2 M methanolic ammonia/DCM) gave the title compound as a colorless oil (70 mg). 1H NMR (400 MHz, CDCl3): 7.19 (d, J=8.6 Hz, 2H), 6.85 (d, J=8.6 Hz, 2H), 3.99 (t, J=6.4 Hz, 2H), 3.35 (s, 2H), 2.50–2.35 (m, 6H), 2.22 (s, 6H), 2.01–1.94 (m, 2H), 1.63–1.55 (m, 4H), 1.46–1.40 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186732B2
Source datasetuspto-grants-2007_03
ORD IDord-d72aa23dc6e241c0a8dccca700e25a1a
Source noteuspto-grants-2007_03