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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33731Generated: October 29, 2026

Dichloromethane → Ammonia dichloromethane

https://huagongshe.com/reaction/33731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant1-IsopropylpiperazineHCID 78013—
Reactant4-(3-Piperidin-1-ylpropoxy)benzaldehydeHCID 2766324—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
Product1-Isopropyl-4-[4-(3-piperidin-1-yl-propoxy)-benzyl]-piperazineHCID 10155403—
ProductAmmonia dichloromethaneHCID 227314291%

Reaction Steps

A solution of the product of Example 9 (200 mg), 1-isopropyl-piperazine (100 mg), and acetic acid (0.05 mL) in DCM (3 mL) was treated with sodium triacetoxyborohydride (290 mg). After 16 h, the resulting mixture was treated with 10% sodium hydroxide (5 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 (225 mg). 1H NMR (400 MHz, CDCl3): 7.19 (d, J=8.6 Hz, 2H), 6.83 (d, J=8.6 Hz, 2H), 3.98 (t, J=6.6 Hz, 2H), 3.43 (s, 2H), 2.63 (m, 1H), 2.53 (br, 4H), 2.46 (m, 4H), 2.39 (br, 4H), 1.96 (m, 2H), 1.58 (m, 4H), 1.46-1.40 (m, 2H), 1.03 (d, J=6.5 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429586B2
Source datasetuspto-grants-2008_09
ORD IDord-59ed4c5836a74af7b0dc4532aaac0233
Source noteuspto-grants-2008_09